Canonical Allele Identifier: CA820492361

Gene: SAMD5

Linked Data

• dbSNP Id: rs1437143065
• gnomAD v3: 6-147796103-G-T
• gnomAD v4: 6-147796103-G-T
• MyVariant Identifiers: chr6:g.148117239G>T (hg19) ; chr6:g.147796103G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796103G>T , CM000668.2:g.147796103G>T	GRCh38
NC_000006.11:g.148117239G>T , CM000668.1:g.148117239G>T	GRCh37
NC_000006.10:g.148158932G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151369G>T	XP_016866339.1:n.460-151369G>T