Canonical Allele Identifier: CA1106522437
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1791909050
gnomAD v3: 7-120665090-G-A
gnomAD v4: 7-120665090-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665090G>A , CM000669.2:g.120665090G>A GRCh38
NC_000007.13:g.120305144G>A , CM000669.1:g.120305144G>A GRCh37
NC_000007.12:g.120092380G>A NCBI36
NG_034230.1:g.396423G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67813G>A MANE Select ENSP00000333496.4:n.1116-67813G>A
ENST00000331113.8:c.1116-67813G>A ENSP00000333496.4:n.1116-67813G>A
NM_012281.2:c.1116-67813G>A NP_036413.1:n.1116-67813G>A
NM_012281.3:c.1116-67813G>A MANE Select NP_036413.1:n.1116-67813G>A
Search 100 bp 5'
Search 100 bp 3'