Canonical Allele Identifier: CA571284233
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1453841561
gnomAD v2: 6-148116608-A-T
gnomAD v3: 6-147795472-A-T
gnomAD v4: 6-147795472-A-T
MyVariant Identifiers: chr6:g.148116608A>T (hg19) chr6:g.147795472A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795472A>T , CM000668.2:g.147795472A>T GRCh38
NC_000006.11:g.148116608A>T , CM000668.1:g.148116608A>T GRCh37
NC_000006.10:g.148158301A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-152000A>T XP_016866339.1:n.460-152000A>T
Search 100 bp 5'
Search 100 bp 3'