Canonical Allele Identifier: CA759453841
Gene: CYTIP HGNC NCBI

Linked Data

dbSNP Id: rs1220301233
MyVariant Identifiers: chr2:g.158278233G>T (hg19) chr2:g.157421721G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421721G>T , CM000664.2:g.157421721G>T GRCh38
NC_000002.11:g.158278233G>T , CM000664.1:g.158278233G>T GRCh37
NC_000002.10:g.157986479G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264192.8:c.547-3132C>A MANE Select ENSP00000264192.3:n.547-3132C>A
ENST00000264192.7:c.547-3132C>A ENSP00000264192.3:n.547-3132C>A
ENST00000418920.5:c.229-3132C>A ENSP00000394308.1:n.229-3132C>A
ENST00000457793.6:c.*442-3132C>A ENSP00000407205.2:n.*442-3132C>A
NM_004288.4:c.547-3132C>A NP_004279.3:n.547-3132C>A
XM_017005386.2:c.229-3132C>A XP_016860875.1:n.229-3132C>A
NM_004288.5:c.547-3132C>A MANE Select NP_004279.3:n.547-3132C>A
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