Canonical Allele Identifier: CA1095587996
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792686020
gnomAD v3: 6-147796104-C-T
gnomAD v4: 6-147796104-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796104C>T , CM000668.2:g.147796104C>T GRCh38
NC_000006.11:g.148117240C>T , CM000668.1:g.148117240C>T GRCh37
NC_000006.10:g.148158933C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151368C>T XP_016866339.1:n.460-151368C>T
Search 100 bp 5'
Search 100 bp 3'