Canonical Allele Identifier: CA1726763486
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415279T= , CM000669.2:g.94415279T= GRCh38
NC_000007.13:g.94044591T= , CM000669.1:g.94044591T= GRCh37
NC_000007.12:g.93882527T= NCBI36
NG_007405.1:g.25719T= , LRG_2:g.25719T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1764+9T= MANE Select ENSP00000297268.6:n.1764+9T=
ENST00000297268.10:c.1764+9T= ENSP00000297268.6:n.1764+9T=
ENST00000473573.5:n.101+9T=
ENST00000488298.5:n.188+9T=
ENST00000620463.1:c.1758+9T= ENSP00000477719.1:n.1758+9T=
NM_000089.3:c.1764+9T= , LRG_2t1:c.1764+9T= NP_000080.2:n.1764+9T=
NM_000089.4:c.1764+9T= MANE Select NP_000080.2:n.1764+9T=
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