Canonical Allele Identifier: CA372803646
Gene: KCNV2 HGNC NCBI
PUM3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2729611T>A (hg19) chr9:g.2729611T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729611T>A , CM000671.2:g.2729611T>A GRCh38
NC_000009.11:g.2729611T>A , CM000671.1:g.2729611T>A GRCh37
NC_000009.10:g.2719611T>A NCBI36
NG_012181.1:g.17086T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.1522T>A (KCNV2) MANE Select ENSP00000371514.3:p.Tyr508Asn
ENST00000382082.3:c.1522T>A (KCNV2) ENSP00000371514.3:p.Tyr508Asn
ENST00000490444.2:c.277-9079A>T (PUM3) ENSP00000474467.1:n.277-9079A>T
NM_133497.3:c.1522T>A (KCNV2) NP_598004.1:p.Tyr508Asn
NM_133497.4:c.1522T>A (KCNV2) MANE Select NP_598004.1:p.Tyr508Asn
Search 100 bp 5'
Search 100 bp 3'