Canonical Allele Identifier: CA456490313
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94055740A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426428A>T , CM000669.2:g.94426428A>T GRCh38
NC_000007.13:g.94055740A>T , CM000669.1:g.94055740A>T GRCh37
NC_000007.12:g.93893676A>T NCBI36
NG_007405.1:g.36868A>T , LRG_2:g.36868A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3003A>T MANE Select ENSP00000297268.6:p.Pro1001=
ENST00000297268.10:c.3003A>T ENSP00000297268.6:p.Pro1001=
ENST00000478215.1:n.562A>T
ENST00000481570.5:n.2976A>T
ENST00000620463.1:c.2997A>T ENSP00000477719.1:p.Pro999=
NM_000089.3:c.3003A>T , LRG_2t1:c.3003A>T NP_000080.2:p.Pro1001=
NM_000089.4:c.3003A>T MANE Select NP_000080.2:p.Pro1001=
Search 100 bp 5'
Search 100 bp 3'