Canonical Allele Identifier: CA500842516
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1286205062
MyVariant Identifiers: chr17:g.48262776G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185415G>C , CM000679.2:g.50185415G>C GRCh38
NC_000017.10:g.48262776G>C , CM000679.1:g.48262776G>C GRCh37
NC_000017.9:g.45617775G>C NCBI36
NG_007400.1:g.21225C>G , LRG_1:g.21225C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.*87C>G MANE Select ENSP00000225964.6:n.*87C>G
ENST00000225964.9:c.*87C>G ENSP00000225964.5:n.*87C>G
NM_000088.3:c.*87C>G , LRG_1t1:c.*87C>G NP_000079.2:n.*87C>G
XM_005257058.3:c.*87C>G XP_005257115.2:n.*87C>G
XM_005257059.3:c.*87C>G XP_005257116.2:n.*87C>G
XM_011524341.1:c.*87C>G XP_011522643.1:n.*87C>G
XM_005257058.4:c.*87C>G XP_005257115.2:n.*87C>G
XM_005257059.4:c.*87C>G XP_005257116.2:n.*87C>G
NM_000088.4:c.*87C>G MANE Select NP_000079.2:n.*87C>G