Canonical Allele Identifier: CA832359006
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1432082525
MyVariant Identifiers: chr7:g.120305147A>C (hg19) chr7:g.120665093A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67810A>C MANE Select ENSP00000333496.4:n.1116-67810A>C
ENST00000331113.8:c.1116-67810A>C ENSP00000333496.4:n.1116-67810A>C
NM_012281.2:c.1116-67810A>C NP_036413.1:n.1116-67810A>C
NM_012281.3:c.1116-67810A>C MANE Select NP_036413.1:n.1116-67810A>C
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