Linked Data
dbSNP Id:
rs977939327
gnomAD v3:
19-2274889-G-T
gnomAD v4:
19-2274889-G-T
MyVariant Identifiers:
chr19:g.2274889G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2274889G>T , CM000681.2:g.2274889G>T | GRCh38 |
| NC_000019.9:g.2274888G>T , CM000681.1:g.2274888G>T | GRCh37 |
| NC_000019.8:g.2225888G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342063.5:c.*791C>A MANE Select | ENSP00000345102.3:n.*791C>A | |
| ENST00000342063.4:c.*791C>A | ENSP00000345102.3:n.*791C>A | |
| ENST00000621615.1:c.146+5145G>T | ENSP00000481965.1:n.146+5145G>T | |
| NM_198532.2:c.*791C>A | NP_940934.1:n.*791C>A | |
| NM_198532.3:c.*791C>A MANE Select | NP_940934.1:n.*791C>A |