Canonical Allele Identifier: CA101609471
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99265219A>T , CM000666.2:g.99265219A>T GRCh38
NC_000004.11:g.100186376A>T , CM000666.1:g.100186376A>T GRCh37
NC_000004.10:g.100405399A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037884.1:n.3790-21576A>T