Canonical Allele Identifier: CA1840046588
Community Standard Title: NC_000009.12:g.23557229T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.23557229T= , CM000671.2:g.23557229T= GRCh38
NC_000009.11:g.23557227T= , CM000671.1:g.23557227T= GRCh37
NC_000009.10:g.23547227T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121602.1:n.1847-2612A=