Linked Data
dbSNP Id:
rs1599874035
gnomAD v4:
19-7125310-G-A
MyVariant Identifiers:
chr19:g.7125321G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7125310G>A , CM000681.2:g.7125310G>A | GRCh38 |
| NC_000019.9:g.7125321G>A , CM000681.1:g.7125321G>A | GRCh37 |
| NC_000019.8:g.7076321G>A | NCBI36 |
| NG_008852.2:g.173691C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.3231C>T MANE Select | ENSP00000303830.4:p.Val1077= | |
| ENST00000302850.9:c.3231C>T | ENSP00000303830.4:p.Val1077= | |
| ENST00000341500.9:c.3195C>T | ENSP00000342838.4:p.Val1065= | |
| ENST00000593970.1:n.77C>T | ||
| NM_000208.2:c.3231C>T | NP_000199.2:p.Val1077= | |
| NM_000208.3:c.3231C>T | NP_000199.2:p.Val1077= | |
| NM_001079817.1:c.3195C>T | NP_001073285.1:p.Val1065= | |
| NM_001079817.2:c.3195C>T | NP_001073285.1:p.Val1065= | |
| XM_011527988.1:c.3306C>T | XP_011526290.1:p.Val1102= | |
| XM_011527989.1:c.3270C>T | XP_011526291.1:p.Val1090= | |
| XM_011527988.2:c.3228C>T | XP_011526290.2:p.Val1076= | |
| XM_011527989.3:c.3192C>T | XP_011526291.2:p.Val1064= | |
| NM_000208.4:c.3231C>T MANE Select | NP_000199.2:p.Val1077= | |
| NM_001079817.3:c.3195C>T | NP_001073285.1:p.Val1065= |