Canonical Allele Identifier: CA1738824619
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1562902875
gnomAD v3: 7-120665087-C-A
gnomAD v4: 7-120665087-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665087C>A , CM000669.2:g.120665087C>A GRCh38
NC_000007.13:g.120305141C>A , CM000669.1:g.120305141C>A GRCh37
NC_000007.12:g.120092377C>A NCBI36
NG_034230.1:g.396420C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67816C>A MANE Select ENSP00000333496.4:n.1116-67816C>A
ENST00000331113.8:c.1116-67816C>A ENSP00000333496.4:n.1116-67816C>A
NM_012281.2:c.1116-67816C>A NP_036413.1:n.1116-67816C>A
NM_012281.3:c.1116-67816C>A MANE Select NP_036413.1:n.1116-67816C>A
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