Canonical Allele Identifier: CA2605087168
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs2128464400

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795736T>G , CM000668.2:g.147795736T>G GRCh38
NC_000006.11:g.148116872T>G , CM000668.1:g.148116872T>G GRCh37
NC_000006.10:g.148158565T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151736T>G XP_016866339.1:n.460-151736T>G