Canonical Allele Identifier: CA1671216669
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792679801

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795744T>G , CM000668.2:g.147795744T>G GRCh38
NC_000006.11:g.148116880T>G , CM000668.1:g.148116880T>G GRCh37
NC_000006.10:g.148158573T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151728T>G XP_016866339.1:n.460-151728T>G