Canonical Allele Identifier: CA2689246205

Linked Data

gnomAD v4: 9-2729895-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729895G>T , CM000671.2:g.2729895G>T GRCh38
NC_000009.11:g.2729895G>T , CM000671.1:g.2729895G>T GRCh37
NC_000009.10:g.2719895G>T NCBI36
NG_012181.1:g.17370G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.*168G>T (KCNV2) MANE Select ENSP00000371514.3:n.*168G>T
ENST00000382082.3:c.*168G>T (KCNV2) ENSP00000371514.3:n.*168G>T
ENST00000490444.2:c.277-9363C>A (PUM3) ENSP00000474467.1:n.277-9363C>A
NM_133497.3:c.*168G>T (KCNV2) NP_598004.1:n.*168G>T
NM_133497.4:c.*168G>T (KCNV2) MANE Select NP_598004.1:n.*168G>T