Canonical Allele Identifier: CA59243169
Gene: CYTIP HGNC NCBI

Linked Data

dbSNP Id: rs990204023
MyVariant Identifiers: chr2:g.158278219G>A (hg19) chr2:g.157421707G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421707G>A , CM000664.2:g.157421707G>A GRCh38
NC_000002.11:g.158278219G>A , CM000664.1:g.158278219G>A GRCh37
NC_000002.10:g.157986465G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264192.8:c.547-3118C>T MANE Select ENSP00000264192.3:n.547-3118C>T
ENST00000264192.7:c.547-3118C>T ENSP00000264192.3:n.547-3118C>T
ENST00000418920.5:c.229-3118C>T ENSP00000394308.1:n.229-3118C>T
ENST00000457793.6:c.*442-3118C>T ENSP00000407205.2:n.*442-3118C>T
NM_004288.4:c.547-3118C>T NP_004279.3:n.547-3118C>T
XM_017005386.2:c.229-3118C>T XP_016860875.1:n.229-3118C>T
NM_004288.5:c.547-3118C>T MANE Select NP_004279.3:n.547-3118C>T
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