Canonical Allele Identifier: CA1671216794
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792683640

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795946A>T , CM000668.2:g.147795946A>T GRCh38
NC_000006.11:g.148117082A>T , CM000668.1:g.148117082A>T GRCh37
NC_000006.10:g.148158775A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151526A>T XP_016866339.1:n.460-151526A>T