Canonical Allele Identifier: CA1095587634
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1390676297

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795724C>T , CM000668.2:g.147795724C>T GRCh38
NC_000006.11:g.148116860C>T , CM000668.1:g.148116860C>T GRCh37
NC_000006.10:g.148158553C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151748C>T XP_016866339.1:n.460-151748C>T