Canonical Allele Identifier: CA368224116
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94052401A>T (hg19) chr7:g.94423089A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423089A>T , CM000669.2:g.94423089A>T GRCh38
NC_000007.13:g.94052401A>T , CM000669.1:g.94052401A>T GRCh37
NC_000007.12:g.93890337A>T NCBI36
NG_007405.1:g.33529A>T , LRG_2:g.33529A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2536A>T MANE Select ENSP00000297268.6:p.Lys846Ter
ENST00000297268.10:c.2536A>T ENSP00000297268.6:p.Lys846Ter
ENST00000481570.5:n.619A>T
ENST00000497316.5:n.933A>T
ENST00000620463.1:c.2530A>T ENSP00000477719.1:p.Lys844Ter
NM_000089.3:c.2536A>T , LRG_2t1:c.2536A>T NP_000080.2:p.Lys846Ter
NM_000089.4:c.2536A>T MANE Select NP_000080.2:p.Lys846Ter
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