Linked Data
ClinVar Variation Id:
1148046
ClinVar RCV Id:
RCV001487770
dbSNP Id:
rs2115033457
MyVariant Identifiers:
chr6:g.129511379T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129190234T>C , CM000668.2:g.129190234T>C | GRCh38 |
| NC_000006.11:g.129511379T>C , CM000668.1:g.129511379T>C | GRCh37 |
| NC_000006.10:g.129553072T>C | NCBI36 |
| NG_008678.1:g.312094T>C , LRG_409:g.312094T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.1497T>C | ENSP00000481744.2:p.Arg499= | |
| ENST00000618192.5:c.1497T>C | ENSP00000480802.2:p.Arg499= | |
| ENST00000686599.1:n.1602T>C | ||
| ENST00000690881.1:n.960T>C | ||
| ENST00000421865.3:c.1497T>C MANE Select | ENSP00000400365.2:p.Arg499= | |
| ENST00000421865.2:c.1497T>C | ENSP00000400365.2:p.Arg499= | |
| ENST00000617695.4:c.1497T>C | ENSP00000481744.1:p.Arg499= | |
| ENST00000618192.4:c.1497T>C | ENSP00000480802.1:p.Arg499= | |
| NM_000426.3:c.1497T>C , LRG_409t1:c.1497T>C | NP_000417.2:p.Arg499= | |
| NM_001079823.1:c.1497T>C | NP_001073291.1:p.Arg499= | |
| XM_005266981.2:c.1497T>C | XP_005267038.1:p.Arg499= | |
| XM_005266982.2:c.1497T>C | XP_005267039.1:p.Arg499= | |
| XM_011535820.1:c.1497T>C | XP_011534122.1:p.Arg499= | |
| XM_005266981.3:c.1497T>C | XP_005267038.1:p.Arg499= | |
| XM_005266982.3:c.1497T>C | XP_005267039.1:p.Arg499= | |
| XM_011535820.2:c.1497T>C | XP_011534122.1:p.Arg499= | |
| XM_017010851.2:c.1503T>C | XP_016866340.1:p.Arg501= | |
| XM_017010853.1:c.1497T>C | XP_016866342.1:p.Arg499= | |
| NM_000426.4:c.1497T>C MANE Select | NP_000417.3:p.Arg499= | |
| NM_001079823.2:c.1497T>C | NP_001073291.2:p.Arg499= |