Canonical Allele Identifier: CA2492005167
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843959T= , CM000664.2:g.17843959T= GRCh38
NC_000002.11:g.18025226T= , CM000664.1:g.18025226T= GRCh37
NC_000002.10:g.17888707T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3735A=