Canonical Allele Identifier: CA843996752
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1400308064
MyVariant Identifiers: chr7:g.94030526T>A (hg19) chr7:g.94401214T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401214T>A , CM000669.2:g.94401214T>A GRCh38
NC_000007.13:g.94030526T>A , CM000669.1:g.94030526T>A GRCh37
NC_000007.12:g.93868462T>A NCBI36
NG_007405.1:g.11654T>A , LRG_2:g.11654T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-353T>A MANE Select ENSP00000297268.6:n.226-353T>A
ENST00000297268.10:c.226-353T>A ENSP00000297268.6:n.226-353T>A
ENST00000620463.1:c.220-353T>A ENSP00000477719.1:n.220-353T>A
NM_000089.3:c.226-353T>A , LRG_2t1:c.226-353T>A NP_000080.2:n.226-353T>A
NM_000089.4:c.226-353T>A MANE Select NP_000080.2:n.226-353T>A
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