Linked Data
ClinVar Variation Id:
3046899
ClinVar RCV Id:
RCV004542426
gnomAD v4:
7-19117121-G-T
MyVariant Identifiers:
chr7:g.19156744G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117121G>T , CM000669.2:g.19117121G>T | GRCh38 |
| NC_000007.13:g.19156744G>T , CM000669.1:g.19156744G>T | GRCh37 |
| NC_000007.12:g.19123269G>T | NCBI36 |
| NG_008114.1:g.5552C>A | |
| NG_008114.2:g.5552C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.201C>A MANE Select | ENSP00000242261.5:p.Gly67= | |
| ENST00000242261.5:c.201C>A | ENSP00000242261.5:p.Gly67= | |
| NM_000474.3:c.201C>A | NP_000465.1:p.Gly67= | |
| XM_011515496.1:c.201C>A | XP_011513798.1:p.Gly67= | |
| NR_149001.1:n.552C>A | ||
| NM_000474.4:c.201C>A MANE Select | NP_000465.1:p.Gly67= | |
| NR_149001.2:n.516C>A |