Canonical Allele Identifier: CA165821475
Gene: KCND2 HGNC NCBI
COSMIC:
COSN20350797 (not active)
MyVariant.info:
GRCh38 chr7:g.120665095G>A
GRCh37 chr7:g.120305149G>A
gnomAD v2:
7:120305149 G / A
gnomAD v3:
7:120665095 G / A
gnomAD v4:
chr7-120665095-G-A
Joint Max Group AF 0.40650583 (EAS)
Genomes Max Group AF 0.40650583 (EAS)
dbSNP:
728115
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665095G>A , CM000669.2:g.120665095G>A GRCh38
NC_000007.13:g.120305149G>A , CM000669.1:g.120305149G>A GRCh37
NC_000007.12:g.120092385G>A NCBI36
NG_034230.1:g.396428G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67808G>A MANE Select ENSP00000333496.4:n.1116-67808G>A
ENST00000331113.8:c.1116-67808G>A ENSP00000333496.4:n.1116-67808G>A
NM_012281.2:c.1116-67808G>A NP_036413.1:n.1116-67808G>A
NM_012281.3:c.1116-67808G>A MANE Select NP_036413.1:n.1116-67808G>A
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