Canonical Allele Identifier: CA165821476
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs913775471
MyVariant Identifiers: chr7:g.120305165G>A (hg19) chr7:g.120665111G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665111G>A , CM000669.2:g.120665111G>A GRCh38
NC_000007.13:g.120305165G>A , CM000669.1:g.120305165G>A GRCh37
NC_000007.12:g.120092401G>A NCBI36
NG_034230.1:g.396444G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67792G>A MANE Select ENSP00000333496.4:n.1116-67792G>A
ENST00000331113.8:c.1116-67792G>A ENSP00000333496.4:n.1116-67792G>A
NM_012281.2:c.1116-67792G>A NP_036413.1:n.1116-67792G>A
NM_012281.3:c.1116-67792G>A MANE Select NP_036413.1:n.1116-67792G>A
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