Canonical Allele Identifier: CA1095587773
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1583175768

Genomic Alleles

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

Transcript Alleles

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