Canonical Allele Identifier: CA162914127
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1039915843
MyVariant Identifiers: chr7:g.94033957G>T (hg19) chr7:g.94404645G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404645G>T , CM000669.2:g.94404645G>T GRCh38
NC_000007.13:g.94033957G>T , CM000669.1:g.94033957G>T GRCh37
NC_000007.12:g.93871893G>T NCBI36
NG_007405.1:g.15085G>T , LRG_2:g.15085G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.324+45G>T MANE Select ENSP00000297268.6:n.324+45G>T
ENST00000297268.10:c.324+45G>T ENSP00000297268.6:n.324+45G>T
ENST00000620463.1:c.318+45G>T ENSP00000477719.1:n.318+45G>T
NM_000089.3:c.324+45G>T , LRG_2t1:c.324+45G>T NP_000080.2:n.324+45G>T
NM_000089.4:c.324+45G>T MANE Select NP_000080.2:n.324+45G>T
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