Canonical Allele Identifier: CA456490340
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94426470-G-A
MyVariant Identifiers: chr7:g.94055782G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426470G>A , CM000669.2:g.94426470G>A GRCh38
NC_000007.13:g.94055782G>A , CM000669.1:g.94055782G>A GRCh37
NC_000007.12:g.93893718G>A NCBI36
NG_007405.1:g.36910G>A , LRG_2:g.36910G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3045G>A MANE Select ENSP00000297268.6:p.Gly1015=
ENST00000297268.10:c.3045G>A ENSP00000297268.6:p.Gly1015=
ENST00000478215.1:n.604G>A
ENST00000481570.5:n.3018G>A
ENST00000620463.1:c.3039G>A ENSP00000477719.1:p.Gly1013=
NM_000089.3:c.3045G>A , LRG_2t1:c.3045G>A NP_000080.2:p.Gly1015=
NM_000089.4:c.3045G>A MANE Select NP_000080.2:p.Gly1015=
Search 100 bp 5'
Search 100 bp 3'