Linked Data
dbSNP Id:
rs1708097671
gnomAD v3:
3-38400940-T-G
gnomAD v4:
3-38400940-T-G
MyVariant Identifiers:
chr3:g.38442431T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38400940T>G , CM000665.2:g.38400940T>G | GRCh38 |
| NC_000003.11:g.38442431T>G , CM000665.1:g.38442431T>G | GRCh37 |
| NC_000003.10:g.38417435T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000207870.8:c.1488T>G MANE Select | ENSP00000207870.3:p.Ala496= | |
| ENST00000649234.1:c.*723T>G | ENSP00000497023.1:n.*723T>G | |
| ENST00000650590.1:c.1407T>G | ENSP00000496840.1:p.Ala469= | |
| ENST00000207870.7:c.1488T>G | ENSP00000207870.3:p.Ala496= | |
| ENST00000424034.5:c.*1151T>G | ENSP00000398845.1:n.*1151T>G | |
| ENST00000472721.1:n.365T>G | ||
| NM_005108.3:c.1488T>G | NP_005099.2:p.Ala496= | |
| XM_011534325.1:c.1488T>G | XP_011532627.1:p.Ala496= | |
| XM_011534326.1:c.1407T>G | XP_011532628.1:p.Ala469= | |
| XM_011534327.1:c.1488T>G | XP_011532629.1:p.Ala496= | |
| XM_011534328.1:c.1488T>G | XP_011532630.1:p.Ala496= | |
| XM_011534329.1:c.1488T>G | XP_011532631.1:p.Ala496= | |
| XM_011534330.1:c.1488T>G | XP_011532632.1:p.Ala496= | |
| NM_001349178.1:c.1488T>G | NP_001336107.1:p.Ala496= | |
| NM_001349179.1:c.1077T>G | NP_001336108.1:p.Ala359= | |
| NR_146068.1:n.1405T>G | ||
| XM_011534325.3:c.1488T>G | XP_011532627.1:p.Ala496= | |
| XM_011534327.2:c.1488T>G | XP_011532629.1:p.Ala496= | |
| XM_011534328.3:c.1488T>G | XP_011532630.1:p.Ala496= | |
| XM_011534329.2:c.1488T>G | XP_011532631.1:p.Ala496= | |
| XM_011534330.3:c.1488T>G | XP_011532632.1:p.Ala496= | |
| XM_017007595.1:c.1077T>G | XP_016863084.1:p.Ala359= | |
| XM_017007596.1:c.1290T>G | XP_016863085.1:p.Ala430= | |
| XM_017007597.1:c.807T>G | XP_016863086.1:p.Ala269= | |
| XM_017007599.2:c.*98T>G | XP_016863088.1:n.*98T>G | |
| XM_024453850.1:c.1290T>G | XP_024309618.1:p.Ala430= | |
| NM_001349178.2:c.1488T>G | NP_001336107.1:p.Ala496= | |
| NM_005108.4:c.1488T>G MANE Select | NP_005099.2:p.Ala496= | |
| NR_146068.2:n.1380T>G | ||
| NM_001349179.2:c.1077T>G | NP_001336108.1:p.Ala359= |