Canonical Allele Identifier: CA1142657161
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682285A= , CM000663.2:g.213682285A= GRCh38
NC_000001.10:g.213855628A= , CM000663.1:g.213855628A= GRCh37
NC_000001.9:g.211922251A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49132A=
XR_001738464.1:n.426-49132A=