Canonical Allele Identifier: CA576321446
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1244646085
gnomAD v2: 7-94030841-T-A
gnomAD v3: 7-94401529-T-A
gnomAD v4: 7-94401529-T-A
MyVariant Identifiers: chr7:g.94030841T>A (hg19) chr7:g.94030841_94030843delinsATA (hg19) chr7:g.94401529T>A (hg38) chr7:g.94401529_94401531delinsATA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401529T>A , CM000669.2:g.94401529T>A GRCh38
NC_000007.13:g.94030841T>A , CM000669.1:g.94030841T>A GRCh37
NC_000007.12:g.93868777T>A NCBI36
NG_007405.1:g.11969T>A , LRG_2:g.11969T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-38T>A MANE Select ENSP00000297268.6:n.226-38T>A
ENST00000297268.10:c.226-38T>A ENSP00000297268.6:n.226-38T>A
ENST00000620463.1:c.220-38T>A ENSP00000477719.1:n.220-38T>A
NM_000089.3:c.226-38T>A , LRG_2t1:c.226-38T>A NP_000080.2:n.226-38T>A
NM_000089.4:c.226-38T>A MANE Select NP_000080.2:n.226-38T>A
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