Canonical Allele Identifier: CA571284322

Gene: SAMD5

Linked Data

• gnomAD v2: 6-148117148-A-C
• gnomAD v3: 6-147796012-A-C
• gnomAD v4: 6-147796012-A-C
• MyVariant Identifiers: chr6:g.148117148A>C (hg19) ; chr6:g.147796012A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.147796012A>C , CM000668.2:g.147796012A>C	GRCh38
NC_000006.11:g.148117148A>C , CM000668.1:g.148117148A>C	GRCh37
NC_000006.10:g.148158841A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010850.1:c.460-151460A>C	XP_016866339.1:n.460-151460A>C