Canonical Allele Identifier: CA372803330

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729467T>C , CM000671.2:g.2729467T>C GRCh38
NC_000009.11:g.2729467T>C , CM000671.1:g.2729467T>C GRCh37
NC_000009.10:g.2719467T>C NCBI36
NG_012181.1:g.16942T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1378T>C (KCNV2) MANE Select ENSP00000371514.3:p.Tyr460His
ENST00000382082.3:c.1378T>C (KCNV2) ENSP00000371514.3:p.Tyr460His
ENST00000490444.2:c.277-8935A>G (PUM3) ENSP00000474467.1:n.277-8935A>G
NM_133497.3:c.1378T>C (KCNV2) NP_598004.1:p.Tyr460His
XR_929202.1:n.2023T>C (KCNV2)
NM_133497.4:c.1378T>C (KCNV2) MANE Select NP_598004.1:p.Tyr460His