Canonical Allele Identifier: CA820492458
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1290921728
gnomAD v3: 6-147796225-T-A
gnomAD v4: 6-147796225-T-A
MyVariant Identifiers: chr6:g.148117361T>A (hg19) chr6:g.147796225T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796225T>A , CM000668.2:g.147796225T>A GRCh38
NC_000006.11:g.148117361T>A , CM000668.1:g.148117361T>A GRCh37
NC_000006.10:g.148159054T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151247T>A XP_016866339.1:n.460-151247T>A
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