Canonical Allele Identifier: CA2683766778
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94401528-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401528T>A , CM000669.2:g.94401528T>A GRCh38
NC_000007.13:g.94030840T>A , CM000669.1:g.94030840T>A GRCh37
NC_000007.12:g.93868776T>A NCBI36
NG_007405.1:g.11968T>A , LRG_2:g.11968T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-39T>A MANE Select ENSP00000297268.6:n.226-39T>A
ENST00000297268.10:c.226-39T>A ENSP00000297268.6:n.226-39T>A
ENST00000620463.1:c.220-39T>A ENSP00000477719.1:n.220-39T>A
NM_000089.3:c.226-39T>A , LRG_2t1:c.226-39T>A NP_000080.2:n.226-39T>A
NM_000089.4:c.226-39T>A MANE Select NP_000080.2:n.226-39T>A