Canonical Allele Identifier: CA1468682071
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553990A= , CM000666.2:g.74553990A= GRCh38
NC_000004.11:g.75419707A= , CM000666.1:g.75419707A= GRCh37
NC_000004.10:g.75638571A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1158T=