Canonical Allele Identifier: CA59243174
Gene: CYTIP HGNC NCBI

Linked Data

dbSNP Id: rs995510424
MyVariant Identifiers: chr2:g.157421768G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421768G>T , CM000664.2:g.157421768G>T GRCh38
NC_000002.11:g.158278280G>T , CM000664.1:g.158278280G>T GRCh37
NC_000002.10:g.157986526G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264192.8:c.547-3179C>A MANE Select ENSP00000264192.3:n.547-3179C>A
ENST00000264192.7:c.547-3179C>A ENSP00000264192.3:n.547-3179C>A
ENST00000418920.5:c.229-3179C>A ENSP00000394308.1:n.229-3179C>A
ENST00000457793.6:c.*442-3179C>A ENSP00000407205.2:n.*442-3179C>A
NM_004288.4:c.547-3179C>A NP_004279.3:n.547-3179C>A
XM_017005386.2:c.229-3179C>A XP_016860875.1:n.229-3179C>A
NM_004288.5:c.547-3179C>A MANE Select NP_004279.3:n.547-3179C>A