Canonical Allele Identifier: CA12629274
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs16148

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282719T>C , CM000669.2:g.24282719T>C GRCh38
NC_000007.12:g.24288863T>C NCBI36
NC_000007.13:g.24322338T>C , CM000669.1:g.24322338T>C GRCh37
NG_016148.1:g.3532T>C

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27020A>G XP_016868399.1:p.=
XM_017012911.1:c.42-27020A>G XP_016868400.1:p.=
XR_001745121.1:n.473+36638A>G
XR_001745122.1:n.345-85690A>G
XR_001745123.1:n.473+36638A>G
XR_001745124.1:n.473+36638A>G
XR_001745125.1:n.473+36638A>G
XR_001745126.1:n.473+36638A>G
XR_001745127.1:n.345-27020A>G
XR_001745129.1:n.473+36638A>G
XR_001745130.1:n.473+36638A>G
XR_001745131.1:n.473+36638A>G
XR_001745132.1:n.473+36638A>G