Canonical Allele Identifier: CA1502599279
Gene:

Linked Data

dbSNP Id: rs1731230513

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649560A>G , CM000666.2:g.148649560A>G GRCh38
NC_000004.11:g.149570712A>G , CM000666.1:g.149570712A>G GRCh37
NC_000004.10:g.149790162A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30692T>C
XR_001741441.1:n.1745+104976A>G
XR_939336.3:n.2921-30692T>C