Canonical Allele Identifier: CA367015608
Gene: TWIST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474221
ClinVar RCV Id: RCV001971103 RCV004553603
dbSNP Id: rs1233220987
MyVariant Identifiers: chr7:g.19156587G>C (hg19) chr7:g.19116964G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.19116964G>C , CM000669.2:g.19116964G>C GRCh38
NC_000007.13:g.19156587G>C , CM000669.1:g.19156587G>C GRCh37
NC_000007.12:g.19123112G>C NCBI36
NG_008114.1:g.5709C>G
NG_008114.2:g.5709C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242261.6:c.358C>G MANE Select ENSP00000242261.5:p.Arg120Gly
ENST00000242261.5:c.358C>G ENSP00000242261.5:p.Arg120Gly
ENST00000354571.5:c.155C>G
NM_000474.3:c.358C>G NP_000465.1:p.Arg120Gly
XM_011515496.1:c.358C>G XP_011513798.1:p.Arg120Gly
NR_149001.1:n.709C>G
NM_000474.4:c.358C>G MANE Select NP_000465.1:p.Arg120Gly
NR_149001.2:n.673C>G
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