Canonical Allele Identifier: CA830507918
Gene: ACTL6B HGNC NCBI

Linked Data

dbSNP Id: rs1203124103

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100646917A>C , CM000669.2:g.100646917A>C GRCh38
NC_000007.13:g.100244540A>C , CM000669.1:g.100244540A>C GRCh37
NC_000007.12:g.100082476A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000160382.10:c.936+54T>G MANE Select ENSP00000160382.5:n.936+54T>G
ENST00000160382.9:c.936+54T>G ENSP00000160382.5:n.936+54T>G
ENST00000487125.1:n.498+54T>G
NM_016188.4:c.936+54T>G NP_057272.1:n.936+54T>G
XR_927476.1:n.1043+54T>G
NR_134539.1:n.1043+54T>G
NM_016188.5:c.936+54T>G MANE Select NP_057272.1:n.936+54T>G
NR_134539.2:n.1030+54T>G