Canonical Allele Identifier: CA372803351
Gene: KCNV2 HGNC NCBI
PUM3 HGNC NCBI

Linked Data

dbSNP Id: rs773096508
gnomAD v3: 9-2729477-T-A
gnomAD v4: 9-2729477-T-A
MyVariant Identifiers: chr9:g.2729477T>A (hg19) chr9:g.2729477T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729477T>A , CM000671.2:g.2729477T>A GRCh38
NC_000009.11:g.2729477T>A , CM000671.1:g.2729477T>A GRCh37
NC_000009.10:g.2719477T>A NCBI36
NG_012181.1:g.16952T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1388T>A (KCNV2) MANE Select ENSP00000371514.3:p.Met463Lys
ENST00000382082.3:c.1388T>A (KCNV2) ENSP00000371514.3:p.Met463Lys
ENST00000490444.2:c.277-8945A>T (PUM3) ENSP00000474467.1:n.277-8945A>T
NM_133497.3:c.1388T>A (KCNV2) NP_598004.1:p.Met463Lys
XR_929202.1:n.2033T>A (KCNV2)
NM_133497.4:c.1388T>A (KCNV2) MANE Select NP_598004.1:p.Met463Lys
Search 100 bp 5'
Search 100 bp 3'