Canonical Allele Identifier: CA1095587776
Gene: SAMD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795916T>C , CM000668.2:g.147795916T>C GRCh38
NC_000006.11:g.148117052T>C , CM000668.1:g.148117052T>C GRCh37
NC_000006.10:g.148158745T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151556T>C XP_016866339.1:n.460-151556T>C