Canonical Allele Identifier: CA832359002
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1354147191
MyVariant Identifiers: chr7:g.120305137T>G (hg19) chr7:g.120665083T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665083T>G , CM000669.2:g.120665083T>G GRCh38
NC_000007.13:g.120305137T>G , CM000669.1:g.120305137T>G GRCh37
NC_000007.12:g.120092373T>G NCBI36
NG_034230.1:g.396416T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67820T>G MANE Select ENSP00000333496.4:n.1116-67820T>G
ENST00000331113.8:c.1116-67820T>G ENSP00000333496.4:n.1116-67820T>G
NM_012281.2:c.1116-67820T>G NP_036413.1:n.1116-67820T>G
NM_012281.3:c.1116-67820T>G MANE Select NP_036413.1:n.1116-67820T>G
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