Canonical Allele Identifier: CA149529080
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs539903155

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795855A>G , CM000668.2:g.147795855A>G GRCh38
NC_000006.11:g.148116991A>G , CM000668.1:g.148116991A>G GRCh37
NC_000006.10:g.148158684A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151617A>G XP_016866339.1:n.460-151617A>G