Canonical Allele Identifier: CA149529088
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1234747

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795900C>T , CM000668.2:g.147795900C>T GRCh38
NC_000006.11:g.148117036C>T , CM000668.1:g.148117036C>T GRCh37
NC_000006.10:g.148158729C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151572C>T XP_016866339.1:n.460-151572C>T