Canonical Allele Identifier: CA59107082
Gene:

Linked Data

dbSNP Id: rs938860804

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870577T>C , CM000664.2:g.155870577T>C GRCh38
NC_000002.11:g.156727089T>C , CM000664.1:g.156727089T>C GRCh37
NC_000002.10:g.156435335T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3390A>G
XR_001739749.1:n.331-29593A>G
XR_001739750.1:n.331-29593A>G
XR_001739751.1:n.331-29593A>G
XR_923501.2:n.331-3390A>G