Canonical Allele Identifier: CA820492477
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1238131694
gnomAD v3: 6-147796244-T-A
gnomAD v4: 6-147796244-T-A
MyVariant Identifiers: chr6:g.148117380T>A (hg19) chr6:g.147796244T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796244T>A , CM000668.2:g.147796244T>A GRCh38
NC_000006.11:g.148117380T>A , CM000668.1:g.148117380T>A GRCh37
NC_000006.10:g.148159073T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151228T>A XP_016866339.1:n.460-151228T>A
Search 100 bp 5'
Search 100 bp 3'