Canonical Allele Identifier: CA577561157
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1172653572
gnomAD v2: 7-120305079-C-T
MyVariant Identifiers: chr7:g.120305079C>T (hg19) chr7:g.120665025C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665025C>T , CM000669.2:g.120665025C>T GRCh38
NC_000007.13:g.120305079C>T , CM000669.1:g.120305079C>T GRCh37
NC_000007.12:g.120092315C>T NCBI36
NG_034230.1:g.396358C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67878C>T MANE Select ENSP00000333496.4:n.1116-67878C>T
ENST00000331113.8:c.1116-67878C>T ENSP00000333496.4:n.1116-67878C>T
NM_012281.2:c.1116-67878C>T NP_036413.1:n.1116-67878C>T
NM_012281.3:c.1116-67878C>T MANE Select NP_036413.1:n.1116-67878C>T
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