Canonical Allele Identifier: CA14983914
Gene: ARVCF HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1034566

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19996754C>T , CM000684.2:g.19996754C>T GRCh38
NC_000022.10:g.19984277C>T , CM000684.1:g.19984277C>T GRCh37
NC_000022.9:g.18364277C>T NCBI36
NG_023326.1:g.25033G>A

Transcript Alleles

HGVS Amino-acid change
NM_001670.2:c.-18-5942G>A VV NP_001661.1:p.=
XM_005261242.1:c.-18-5942G>A XP_005261299.1:p.=
XM_005261243.3:c.-18-5942G>A XP_005261300.1:p.=
XM_005261244.3:c.-18-5942G>A XP_005261301.1:p.=
XM_006724243.1:c.-18-5942G>A XP_006724306.1:p.=
XM_006724245.2:c.-18-5942G>A XP_006724308.1:p.=
XM_006724249.2:c.-18-5942G>A XP_006724312.1:p.=
XM_006724250.2:c.-18-5942G>A XP_006724313.1:p.=
XM_011530179.1:c.-18-5942G>A XP_011528481.1:p.=
XM_011530180.1:c.-18-5942G>A XP_011528482.1:p.=
XM_011530181.1:c.-18-5942G>A XP_011528483.1:p.=
XR_937863.1:n.269-5942G>A
XR_937864.1:n.269-5942G>A
XM_005261242.3:c.-18-5942G>A
XM_005261243.4:c.-18-5942G>A
XM_005261244.4:c.-18-5942G>A
XM_006724243.3:c.-18-5942G>A
XM_006724245.3:c.-18-5942G>A
XM_006724249.3:c.-18-5942G>A
XM_006724250.3:c.-18-5942G>A
XM_011530179.3:c.-18-5942G>A
XR_937863.2:n.269-5942G>A
NM_001670.3:c.-18-5942G>A VV MANE Preferred
ENST00000263207.7:c.-18-5942G>A ENSP00000263207.3:p.=
ENST00000467828.1:n.158-14663G>A