Canonical Allele Identifier: CA155466597
Gene: TWIST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 802300
ClinVar RCV Id: RCV000987855 RCV001263196 RCV002274112
dbSNP Id: rs104894054
MyVariant Identifiers: chr7:g.19156636G>C (hg19) chr7:g.19117013G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.19117013G>C , CM000669.2:g.19117013G>C GRCh38
NC_000007.13:g.19156636G>C , CM000669.1:g.19156636G>C GRCh37
NC_000007.12:g.19123161G>C NCBI36
NG_008114.1:g.5660C>G
NG_008114.2:g.5660C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242261.6:c.309C>G MANE Select ENSP00000242261.5:p.Tyr103Ter
ENST00000242261.5:c.309C>G ENSP00000242261.5:p.Tyr103Ter
ENST00000354571.5:c.106C>G
NM_000474.3:c.309C>G NP_000465.1:p.Tyr103Ter
XM_011515496.1:c.309C>G XP_011513798.1:p.Tyr103Ter
NR_149001.1:n.660C>G
NM_000474.4:c.309C>G MANE Select NP_000465.1:p.Tyr103Ter
NR_149001.2:n.624C>G
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