Canonical Allele Identifier: CA12691106
Gene: ACTR3B HGNC NCBI

Linked Data

dbSNP Id: rs11981919
gnomAD v2: 7-152669840-G-A
gnomAD v3: 7-152972755-G-A
gnomAD v4: 7-152972755-G-A
MyVariant Identifiers: chr7:g.152669840G>A (hg19) chr7:g.152972755G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152972755G>A , CM000669.2:g.152972755G>A GRCh38
NC_000007.13:g.152669840G>A , CM000669.1:g.152669840G>A GRCh37
NC_000007.12:g.152300773G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017012460.1:c.952-90842G>A XP_016867949.1:n.952-90842G>A
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