Canonical Allele Identifier: CA820492462
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1226492881
gnomAD v3: 6-147796226-C-T
gnomAD v4: 6-147796226-C-T
MyVariant Identifiers: chr6:g.148117362C>T (hg19) chr6:g.147796226C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796226C>T , CM000668.2:g.147796226C>T GRCh38
NC_000006.11:g.148117362C>T , CM000668.1:g.148117362C>T GRCh37
NC_000006.10:g.148159055C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151246C>T XP_016866339.1:n.460-151246C>T
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