Canonical Allele Identifier: CA1671216778
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792683249

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795913G>T , CM000668.2:g.147795913G>T GRCh38
NC_000006.11:g.148117049G>T , CM000668.1:g.148117049G>T GRCh37
NC_000006.10:g.148158742G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151559G>T XP_016866339.1:n.460-151559G>T