Canonical Allele Identifier: CA149529063
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1034582840
gnomAD v2: 6-148116767-G-A
gnomAD v3: 6-147795631-G-A
gnomAD v4: 6-147795631-G-A
MyVariant Identifiers: chr6:g.148116767G>A (hg19) chr6:g.147795631G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795631G>A , CM000668.2:g.147795631G>A GRCh38
NC_000006.11:g.148116767G>A , CM000668.1:g.148116767G>A GRCh37
NC_000006.10:g.148158460G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151841G>A XP_016866339.1:n.460-151841G>A
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