Canonical Allele Identifier: CA456486817
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94401611-T-A
MyVariant Identifiers: chr7:g.94030923T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401611T>A , CM000669.2:g.94401611T>A GRCh38
NC_000007.13:g.94030923T>A , CM000669.1:g.94030923T>A GRCh37
NC_000007.12:g.93868859T>A NCBI36
NG_007405.1:g.12051T>A , LRG_2:g.12051T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.270T>A MANE Select ENSP00000297268.6:p.Pro90=
ENST00000297268.10:c.270T>A ENSP00000297268.6:p.Pro90=
ENST00000620463.1:c.264T>A ENSP00000477719.1:p.Pro88=
NM_000089.3:c.270T>A , LRG_2t1:c.270T>A NP_000080.2:p.Pro90=
NM_000089.4:c.270T>A MANE Select NP_000080.2:p.Pro90=
Search 100 bp 5'
Search 100 bp 3'