Canonical Allele Identifier: CA59243173
Gene: CYTIP HGNC NCBI

Linked Data

dbSNP Id: rs3769376
gnomAD v2: 2-158278245-G-C
gnomAD v3: 2-157421733-G-C
gnomAD v4: 2-157421733-G-C
MyVariant Identifiers: chr2:g.158278245G>C (hg19) chr2:g.157421733G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157421733G>C , CM000664.2:g.157421733G>C GRCh38
NC_000002.11:g.158278245G>C , CM000664.1:g.158278245G>C GRCh37
NC_000002.10:g.157986491G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264192.8:c.547-3144C>G MANE Select ENSP00000264192.3:n.547-3144C>G
ENST00000264192.7:c.547-3144C>G ENSP00000264192.3:n.547-3144C>G
ENST00000418920.5:c.229-3144C>G ENSP00000394308.1:n.229-3144C>G
ENST00000457793.6:c.*442-3144C>G ENSP00000407205.2:n.*442-3144C>G
NM_004288.4:c.547-3144C>G NP_004279.3:n.547-3144C>G
XM_017005386.2:c.229-3144C>G XP_016860875.1:n.229-3144C>G
NM_004288.5:c.547-3144C>G MANE Select NP_004279.3:n.547-3144C>G
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