Canonical Allele Identifier: CA1468682057
Gene:

Linked Data

dbSNP Id: rs1721060073

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553974A>T , CM000666.2:g.74553974A>T GRCh38
NC_000004.11:g.75419691A>T , CM000666.1:g.75419691A>T GRCh37
NC_000004.10:g.75638555A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1142T>A