Canonical Allele Identifier: CA1738824655
Gene: KCND2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665093A= , CM000669.2:g.120665093A= GRCh38
NC_000007.13:g.120305147A= , CM000669.1:g.120305147A= GRCh37
NC_000007.12:g.120092383A= NCBI36
NG_034230.1:g.396426A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67810A= MANE Select ENSP00000333496.4:n.1116-67810A=
ENST00000331113.8:c.1116-67810A= ENSP00000333496.4:n.1116-67810A=
NM_012281.2:c.1116-67810A= NP_036413.1:n.1116-67810A=
NM_012281.3:c.1116-67810A= MANE Select NP_036413.1:n.1116-67810A=
Search 100 bp 5'
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