Canonical Allele Identifier: CA1284436092
Gene:

Linked Data

dbSNP Id: rs1573711183

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379273T>A , CM000664.2:g.122379273T>A GRCh38
NC_000002.11:g.123136849T>A , CM000664.1:g.123136849T>A GRCh37
NC_000002.10:g.122853319T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13690T>A
XR_001739684.1:n.556-13690T>A