Linked Data
ClinVar Variation Id:
2106348
ClinVar RCV Id:
RCV003026421
gnomAD v4:
5-74685275-G-T
MyVariant Identifiers:
chr5:g.73981100G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74685275G>T , CM000667.2:g.74685275G>T | GRCh38 |
| NC_000005.9:g.73981100G>T , CM000667.1:g.73981100G>T | GRCh37 |
| NC_000005.8:g.74016856G>T | NCBI36 |
| NG_009770.1:g.5132G>T | |
| NG_009770.2:g.50253G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261416.12:c.15G>T MANE Select | ENSP00000261416.7:p.Gly5= | |
| ENST00000261416.11:c.15G>T | ENSP00000261416.7:p.Gly5= | |
| ENST00000511181.5:c.-376-4053G>T | ENSP00000426285.1:n.-376-4053G>T | |
| ENST00000513079.5:n.80G>T | ||
| ENST00000515528.1:n.70G>T | ||
| NM_000521.3:c.15G>T | NP_000512.1:p.Gly5= | |
| NM_001292004.1:c.-376-4053G>T | NP_001278933.1:n.-376-4053G>T | |
| NM_000521.4:c.15G>T MANE Select | NP_000512.2:p.Gly5= | |
| NM_001292004.2:c.-376-4053G>T | NP_001278933.1:n.-376-4053G>T |