Canonical Allele Identifier: CA1671216769
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795905A= , CM000668.2:g.147795905A= GRCh38
NC_000006.11:g.148117041A= , CM000668.1:g.148117041A= GRCh37
NC_000006.10:g.148158734A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151567A= XP_016866339.1:n.460-151567A=