Canonical Allele Identifier: CA2263915126
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1906744591

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188412A>C , CM000679.2:g.50188412A>C GRCh38
NC_000017.10:g.48265773A>C , CM000679.1:g.48265773A>C GRCh37
NC_000017.9:g.45620772A>C NCBI36
NG_007400.1:g.18228T>G , LRG_1:g.18228T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3207+118T>G MANE Select ENSP00000225964.6:n.3207+118T>G
ENST00000225964.9:c.3207+118T>G ENSP00000225964.5:n.3207+118T>G
ENST00000486572.1:n.143T>G
ENST00000511732.1:n.269T>G
NM_000088.3:c.3207+118T>G , LRG_1t1:c.3207+118T>G NP_000079.2:n.3207+118T>G
XM_005257058.3:c.2937+118T>G XP_005257115.2:n.2937+118T>G
XM_005257059.3:c.2289+118T>G XP_005257116.2:n.2289+118T>G
XM_011524341.1:c.3009+118T>G XP_011522643.1:n.3009+118T>G
XM_005257058.4:c.2937+118T>G XP_005257115.2:n.2937+118T>G
XM_005257059.4:c.2289+118T>G XP_005257116.2:n.2289+118T>G
NM_000088.4:c.3207+118T>G MANE Select NP_000079.2:n.3207+118T>G