Canonical Allele Identifier: CA2689245366

Linked Data

gnomAD v4: 9-2729369-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729369C>T , CM000671.2:g.2729369C>T GRCh38
NC_000009.11:g.2729369C>T , CM000671.1:g.2729369C>T GRCh37
NC_000009.10:g.2719369C>T NCBI36
NG_012181.1:g.16844C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-77C>T (KCNV2) MANE Select ENSP00000371514.3:n.1357-77C>T
ENST00000382082.3:c.1357-77C>T (KCNV2) ENSP00000371514.3:n.1357-77C>T
ENST00000490444.2:c.277-8837G>A (PUM3) ENSP00000474467.1:n.277-8837G>A
NM_133497.3:c.1357-77C>T (KCNV2) NP_598004.1:n.1357-77C>T
XR_929202.1:n.2002-77C>T (KCNV2)
XR_929203.1:n.2345C>T (KCNV2)
NM_133497.4:c.1357-77C>T (KCNV2) MANE Select NP_598004.1:n.1357-77C>T