Canonical Allele Identifier: CA1502599377
Gene:

Linked Data

dbSNP Id: rs1731230989

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649593C>A , CM000666.2:g.148649593C>A GRCh38
NC_000004.11:g.149570745C>A , CM000666.1:g.149570745C>A GRCh37
NC_000004.10:g.149790195C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30725G>T
XR_001741441.1:n.1745+105009C>A
XR_939336.3:n.2921-30725G>T