Canonical Allele Identifier: CA820492299

Gene: SAMD5

Linked Data

• dbSNP Id: rs1175482197
• gnomAD v3: 6-147796026-C-G
• gnomAD v4: 6-147796026-C-G
• MyVariant Identifiers: chr6:g.148117162C>G (hg19) ; chr6:g.147796026C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796026C>G , CM000668.2:g.147796026C>G	GRCh38
NC_000006.11:g.148117162C>G , CM000668.1:g.148117162C>G	GRCh37
NC_000006.10:g.148158855C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151446C>G	XP_016866339.1:n.460-151446C>G