Linked Data
ClinVar Variation Id:
2122472
ClinVar RCV Id:
RCV003046886
MyVariant Identifiers:
chr17:g.44109587A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46032221A>G , CM000679.2:g.46032221A>G | GRCh38 |
| NC_000017.10:g.44109587A>G , CM000679.1:g.44109587A>G | GRCh37 |
| NC_000017.9:g.41465434A>G | NCBI36 |
| NG_032784.1:g.198154T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432791.7:c.2916T>C MANE Select | ENSP00000387393.3:p.Pro972= | |
| ENST00000572904.6:c.2916T>C | ENSP00000461484.1:p.Pro972= | |
| ENST00000574590.6:c.2913T>C | ENSP00000461812.2:p.Pro971= | |
| ENST00000575318.6:c.2724T>C | ENSP00000461299.1:p.Pro908= | |
| ENST00000638275.1:c.2724T>C | ENSP00000492576.1:p.Pro908= | |
| ENST00000638291.1:n.744T>C | ||
| ENST00000638551.1:n.864T>C | ||
| ENST00000639467.1:c.573T>C | ENSP00000492741.1:p.Pro191= | |
| ENST00000639805.1:n.333T>C | ||
| ENST00000648792.1:c.2838-54T>C | ENSP00000497628.1:n.2838-54T>C | |
| ENST00000262419.10:c.2916T>C | ENSP00000262419.6:p.Pro972= | |
| ENST00000432791.5:c.2913T>C | ENSP00000387393.2:p.Pro971= | |
| ENST00000572218.5:n.7133T>C | ||
| ENST00000572904.5:c.2916T>C | ENSP00000461484.1:p.Pro972= | |
| ENST00000573682.1:n.302T>C | ||
| ENST00000574590.5:c.2916T>C | ENSP00000461812.1:p.Pro972= | |
| ENST00000574963.1:n.346T>C | ||
| ENST00000575318.5:c.2724T>C | ENSP00000461299.1:p.Pro908= | |
| ENST00000576870.5:n.888T>C | ||
| NM_001193465.1:c.2913T>C | NP_001180394.1:p.Pro971= | |
| NM_001193466.1:c.2916T>C | NP_001180395.1:p.Pro972= | |
| NM_015443.3:c.2916T>C | NP_056258.1:p.Pro972= | |
| XM_006721823.1:c.2916T>C | XP_006721886.1:p.Pro972= | |
| XM_006721824.2:c.2916T>C | XP_006721887.1:p.Pro972= | |
| XM_011524628.1:c.2913T>C | XP_011522930.1:p.Pro971= | |
| XM_011524629.1:c.2814T>C | XP_011522931.1:p.Pro938= | |
| XM_011524630.1:c.2727T>C | XP_011522932.1:p.Pro909= | |
| XM_011524631.1:c.2724T>C | XP_011522933.1:p.Pro908= | |
| XM_011524632.1:c.1686T>C | XP_011522934.1:p.Pro562= | |
| XM_006721823.2:c.2916T>C | XP_006721886.1:p.Pro972= | |
| XM_006721824.4:c.2916T>C | XP_006721887.1:p.Pro972= | |
| XM_011524628.3:c.2913T>C | XP_011522930.1:p.Pro971= | |
| XM_011524629.3:c.2814T>C | XP_011522931.1:p.Pro938= | |
| XM_011524630.3:c.2727T>C | XP_011522932.1:p.Pro909= | |
| XM_011524631.3:c.2724T>C | XP_011522933.1:p.Pro908= | |
| XM_011524632.3:c.1686T>C | XP_011522934.1:p.Pro562= | |
| XM_017024488.2:c.2724T>C | XP_016879977.1:p.Pro908= | |
| NM_001193466.2:c.2916T>C | NP_001180395.1:p.Pro972= | |
| NM_015443.4:c.2916T>C MANE Select | NP_056258.1:p.Pro972= | |
| NM_001193465.2:c.2913T>C | NP_001180394.1:p.Pro971= | |
| NM_001379198.1:c.2916T>C | NP_001366127.1:p.Pro972= |