Canonical Allele Identifier: CA571284327

Gene: SAMD5

Linked Data

• dbSNP Id: rs1228166343
• gnomAD v2: 6-148117170-GT-G
• gnomAD v3: 6-147796034-GT-G
• gnomAD v4: 6-147796034-GT-G
• MyVariant Identifiers: chr6:g.148117171del (hg19) ; chr6:g.147796035del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796035del , CM000668.2:g.147796035del	GRCh38
NC_000006.11:g.148117171del , CM000668.1:g.148117171del	GRCh37
NC_000006.10:g.148158864del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151437del	XP_016866339.1:n.460-151437del