Linked Data
dbSNP Id:
rs2137622669
gnomAD v4:
13-28018476-G-A
MyVariant Identifiers:
chr13:g.28592613G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.28018476G>A , CM000675.2:g.28018476G>A | GRCh38 |
| NC_000013.10:g.28592613G>A , CM000675.1:g.28592613G>A | GRCh37 |
| NC_000013.9:g.27490613G>A | NCBI36 |
| NG_007066.1:g.87093C>T , LRG_457:g.87093C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000241453.12:c.2532C>T MANE Select | ENSP00000241453.7:p.Val844= | |
| ENST00000241453.11:c.2532C>T | ENSP00000241453.7:p.Val844= | |
| ENST00000380987.2:c.*444C>T | ENSP00000370374.2:n.*444C>T | |
| NM_004119.2:c.2532C>T , LRG_457t1:c.2532C>T | NP_004110.2:p.Val844= | |
| NR_130706.1:n.2746C>T | ||
| XM_011535015.1:c.2475C>T | XP_011533317.1:p.Val825= | |
| XM_011535016.1:c.2007C>T | XP_011533318.1:p.Val669= | |
| XM_011535017.1:c.2007C>T | XP_011533319.1:p.Val669= | |
| XM_011535018.1:c.2007C>T | XP_011533320.1:p.Val669= | |
| XM_011535015.2:c.2475C>T | XP_011533317.1:p.Val825= | |
| XM_011535017.2:c.2007C>T | XP_011533319.1:p.Val669= | |
| XM_011535018.2:c.2007C>T | XP_011533320.1:p.Val669= | |
| XM_017020486.1:c.2316C>T | XP_016875975.1:p.Val772= | |
| XM_017020487.1:c.2007C>T | XP_016875976.1:p.Val669= | |
| XM_017020488.1:c.1653C>T | XP_016875977.1:p.Val551= | |
| XM_017020489.1:c.1635C>T | XP_016875978.1:p.Val545= | |
| NM_004119.3:c.2532C>T MANE Select | NP_004110.2:p.Val844= | |
| NR_130706.2:n.2730C>T |