Canonical Allele Identifier: CA165821474
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs987893632
gnomAD v3: 7-120665094-A-G
gnomAD v4: 7-120665094-A-G
MyVariant Identifiers: chr7:g.120305148A>G (hg19) chr7:g.120665094A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665094A>G , CM000669.2:g.120665094A>G GRCh38
NC_000007.13:g.120305148A>G , CM000669.1:g.120305148A>G GRCh37
NC_000007.12:g.120092384A>G NCBI36
NG_034230.1:g.396427A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331113.9:c.1116-67809A>G MANE Select ENSP00000333496.4:n.1116-67809A>G
ENST00000331113.8:c.1116-67809A>G ENSP00000333496.4:n.1116-67809A>G
NM_012281.2:c.1116-67809A>G NP_036413.1:n.1116-67809A>G
NM_012281.3:c.1116-67809A>G MANE Select NP_036413.1:n.1116-67809A>G
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