Canonical Allele Identifier: CA1738824525
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1172653572
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665025C>G , CM000669.2:g.120665025C>G GRCh38
NC_000007.13:g.120305079C>G , CM000669.1:g.120305079C>G GRCh37
NC_000007.12:g.120092315C>G NCBI36
NG_034230.1:g.396358C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67878C>G MANE Select ENSP00000333496.4:n.1116-67878C>G
ENST00000331113.8:c.1116-67878C>G ENSP00000333496.4:n.1116-67878C>G
NM_012281.2:c.1116-67878C>G NP_036413.1:n.1116-67878C>G
NM_012281.3:c.1116-67878C>G MANE Select NP_036413.1:n.1116-67878C>G
Search 100 bp 5'
Search 100 bp 3'