Canonical Allele Identifier: CA165821454
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs778273184

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120664950T>C , CM000669.2:g.120664950T>C GRCh38
NC_000007.13:g.120305004T>C , CM000669.1:g.120305004T>C GRCh37
NC_000007.12:g.120092240T>C NCBI36
NG_034230.1:g.396283T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67953T>C MANE Select ENSP00000333496.4:n.1116-67953T>C
ENST00000331113.8:c.1116-67953T>C ENSP00000333496.4:n.1116-67953T>C
NM_012281.2:c.1116-67953T>C NP_036413.1:n.1116-67953T>C
NM_012281.3:c.1116-67953T>C MANE Select NP_036413.1:n.1116-67953T>C