Canonical Allele Identifier: CA571284301
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1243424888

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795930A>C , CM000668.2:g.147795930A>C GRCh38
NC_000006.11:g.148117066A>C , CM000668.1:g.148117066A>C GRCh37
NC_000006.10:g.148158759A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151542A>C XP_016866339.1:n.460-151542A>C