Canonical Allele Identifier: CA149529097

Gene: SAMD5

Linked Data

• dbSNP Id: rs1034527099
• gnomAD v3: 6-147796132-G-A
• gnomAD v4: 6-147796132-G-A
• MyVariant Identifiers: chr6:g.148117268G>A (hg19) ; chr6:g.147796132G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796132G>A , CM000668.2:g.147796132G>A	GRCh38
NC_000006.11:g.148117268G>A , CM000668.1:g.148117268G>A	GRCh37
NC_000006.10:g.148158961G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151340G>A	XP_016866339.1:n.460-151340G>A