Canonical Allele Identifier: CA4965908

Linked Data

dbSNP Id: rs749491193
gnomAD v2: 9-2729476-A-T
gnomAD v4: 9-2729476-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729476A>T , CM000671.2:g.2729476A>T GRCh38
NC_000009.11:g.2729476A>T , CM000671.1:g.2729476A>T GRCh37
NC_000009.10:g.2719476A>T NCBI36
NG_012181.1:g.16951A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1387A>T (KCNV2) MANE Select ENSP00000371514.3:p.Met463Leu
ENST00000382082.3:c.1387A>T (KCNV2) ENSP00000371514.3:p.Met463Leu
ENST00000490444.2:c.277-8944T>A (PUM3) ENSP00000474467.1:n.277-8944T>A
NM_133497.3:c.1387A>T (KCNV2) NP_598004.1:p.Met463Leu
XR_929202.1:n.2032A>T (KCNV2)
NM_133497.4:c.1387A>T (KCNV2) MANE Select NP_598004.1:p.Met463Leu