Linked Data
dbSNP Id:
rs2086853682
gnomAD v4:
15-44711170-G-C
MyVariant Identifiers:
chr15:g.45003368G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711170G>C , CM000677.2:g.44711170G>C | GRCh38 |
| NC_000015.9:g.45003368G>C , CM000677.1:g.45003368G>C | GRCh37 |
| NC_000015.8:g.42790660G>C | NCBI36 |
| NG_012920.1:g.4684G>C | |
| NG_012920.2:g.4694G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682850.1:c.-404C>G MANE Select | ENSP00000508024.1:n.-404C>G | |
| ENST00000558573.1:n.147C>G | ||
| XM_011521338.1:c.-404C>G | XP_011519640.1:n.-404C>G | |
| XM_011521339.1:c.-285C>G | XP_011519641.1:n.-285C>G | |
| XM_011521340.1:c.-226C>G | XP_011519642.1:n.-226C>G | |
| XM_011521343.1:c.-488C>G | XP_011519645.1:n.-488C>G | |
| XM_011521345.1:c.-459C>G | XP_011519647.1:n.-459C>G | |
| XM_011521338.3:c.-404C>G | XP_011519640.1:n.-404C>G | |
| XM_011521339.3:c.-285C>G | XP_011519641.1:n.-285C>G | |
| XM_011521340.3:c.-226C>G | XP_011519642.1:n.-226C>G | |
| XM_011521343.3:c.-488C>G | XP_011519645.1:n.-488C>G | |
| XM_011521345.3:c.-459C>G | XP_011519647.1:n.-459C>G | |
| NM_001387260.1:c.-76+162C>G | NP_001374189.1:n.-76+162C>G | |
| NM_001387261.1:c.-226C>G | NP_001374190.1:n.-226C>G | |
| NM_001387262.1:c.-494C>G | NP_001374191.1:n.-494C>G | |
| NM_001387263.1:c.-404C>G MANE Select | NP_001374192.1:n.-404C>G |