Canonical Allele Identifier: CA2683767000
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94401770-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401770G>T , CM000669.2:g.94401770G>T GRCh38
NC_000007.13:g.94031082G>T , CM000669.1:g.94031082G>T GRCh37
NC_000007.12:g.93869018G>T NCBI36
NG_007405.1:g.12210G>T , LRG_2:g.12210G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.279+150G>T MANE Select ENSP00000297268.6:n.279+150G>T
ENST00000297268.10:c.279+150G>T ENSP00000297268.6:n.279+150G>T
ENST00000620463.1:c.273+150G>T ENSP00000477719.1:n.273+150G>T
NM_000089.3:c.279+150G>T , LRG_2t1:c.279+150G>T NP_000080.2:n.279+150G>T
NM_000089.4:c.279+150G>T MANE Select NP_000080.2:n.279+150G>T
Search 100 bp 5'
Search 100 bp 3'