Canonical Allele Identifier: CA187990614

Linked Data

dbSNP Id: rs540063630
MyVariant Identifiers: chr9:g.2729799G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729799G>A , CM000671.2:g.2729799G>A GRCh38
NC_000009.11:g.2729799G>A , CM000671.1:g.2729799G>A GRCh37
NC_000009.10:g.2719799G>A NCBI36
NG_012181.1:g.17274G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.*72G>A (KCNV2) MANE Select ENSP00000371514.3:n.*72G>A
ENST00000382082.3:c.*72G>A (KCNV2) ENSP00000371514.3:n.*72G>A
ENST00000490444.2:c.277-9267C>T (PUM3) ENSP00000474467.1:n.277-9267C>T
NM_133497.3:c.*72G>A (KCNV2) NP_598004.1:n.*72G>A
NM_133497.4:c.*72G>A (KCNV2) MANE Select NP_598004.1:n.*72G>A