Canonical Allele Identifier: CA1595022660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333159T= , CM000667.2:g.159333159T= GRCh38
NC_000005.9:g.158760167T= , CM000667.1:g.158760167T= GRCh37
NC_000005.8:g.158692745T= NCBI36
NG_009618.1:g.2315A= , LRG_71:g.2315A=

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+156T=