Canonical Allele Identifier: CA390387937
Gene: LTBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.75078320G>C (hg19) chr14:g.74611617G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74611617G>C , CM000676.2:g.74611617G>C GRCh38
NC_000014.8:g.75078320G>C , CM000676.1:g.75078320G>C GRCh37
NC_000014.7:g.74148073G>C NCBI36
NG_021486.1:g.5715C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261978.9:c.328C>G MANE Select ENSP00000261978.4:p.Gln110Glu
ENST00000261978.8:c.328C>G ENSP00000261978.4:p.Gln110Glu
ENST00000553939.5:c.328C>G ENSP00000452110.1:p.Gln110Glu
ENST00000556690.5:c.328C>G ENSP00000451477.1:p.Gln110Glu
ENST00000557425.1:n.123+429C>G
NM_000428.2:c.328C>G NP_000419.1:p.Gln110Glu
XM_011536765.1:c.328C>G XP_011535067.1:p.Gln110Glu
XM_011536767.1:c.11+6967C>G XP_011535069.1:n.11+6967C>G
XM_011536765.2:c.328C>G XP_011535067.1:p.Gln110Glu
NM_000428.3:c.328C>G MANE Select NP_000419.1:p.Gln110Glu
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