Canonical Allele Identifier: CA1738824616
Gene: KCND2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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