Canonical Allele Identifier: CA820492376

Gene: SAMD5

Linked Data

• dbSNP Id: rs1182129937
• MyVariant Identifiers: chr6:g.148117277C>T (hg19) ; chr6:g.147796141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796141C>T , CM000668.2:g.147796141C>T	GRCh38
NC_000006.11:g.148117277C>T , CM000668.1:g.148117277C>T	GRCh37
NC_000006.10:g.148158970C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151331C>T	XP_016866339.1:n.460-151331C>T