Canonical Allele Identifier: CA1595022649
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333101T= , CM000667.2:g.159333101T= GRCh38
NC_000005.9:g.158760109T= , CM000667.1:g.158760109T= GRCh37
NC_000005.8:g.158692687T= NCBI36
NG_009618.1:g.2373A= , LRG_71:g.2373A=

Transcript Alleles

HGVS Amino-acid change
NR_037889.1:n.745+98T=