Canonical Allele Identifier: CA165821472
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs181582654
gnomAD v3: 7-120665088-C-T
gnomAD v4: 7-120665088-C-T
MyVariant Identifiers: chr7:g.120305142C>T (hg19) chr7:g.120665088C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665088C>T , CM000669.2:g.120665088C>T GRCh38
NC_000007.13:g.120305142C>T , CM000669.1:g.120305142C>T GRCh37
NC_000007.12:g.120092378C>T NCBI36
NG_034230.1:g.396421C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331113.9:c.1116-67815C>T MANE Select ENSP00000333496.4:n.1116-67815C>T
ENST00000331113.8:c.1116-67815C>T ENSP00000333496.4:n.1116-67815C>T
NM_012281.2:c.1116-67815C>T NP_036413.1:n.1116-67815C>T
NM_012281.3:c.1116-67815C>T MANE Select NP_036413.1:n.1116-67815C>T
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