Canonical Allele Identifier: CA463854204

Linked Data

MyVariant Identifiers: chr9:g.2729673A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729673A>C , CM000671.2:g.2729673A>C GRCh38
NC_000009.11:g.2729673A>C , CM000671.1:g.2729673A>C GRCh37
NC_000009.10:g.2719673A>C NCBI36
NG_012181.1:g.17148A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.1584A>C (KCNV2) MANE Select ENSP00000371514.3:p.Ile528=
ENST00000382082.3:c.1584A>C (KCNV2) ENSP00000371514.3:p.Ile528=
ENST00000490444.2:c.277-9141T>G (PUM3) ENSP00000474467.1:n.277-9141T>G
NM_133497.3:c.1584A>C (KCNV2) NP_598004.1:p.Ile528=
NM_133497.4:c.1584A>C (KCNV2) MANE Select NP_598004.1:p.Ile528=