Canonical Allele Identifier: CA500849840
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48272094G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194733G>C , CM000679.2:g.50194733G>C GRCh38
NC_000017.10:g.48272094G>C , CM000679.1:g.48272094G>C GRCh37
NC_000017.9:g.45627093G>C NCBI36
NG_007400.1:g.11907C>G , LRG_1:g.11907C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1449C>G MANE Select ENSP00000225964.6:p.Pro483=
ENST00000225964.9:c.1449C>G ENSP00000225964.5:p.Pro483=
ENST00000471344.1:n.393C>G
NM_000088.3:c.1449C>G , LRG_1t1:c.1449C>G NP_000079.2:p.Pro483=
XM_005257058.3:c.1449C>G XP_005257115.2:p.Pro483=
XM_005257059.3:c.957+1581C>G XP_005257116.2:n.957+1581C>G
XM_011524341.1:c.1251C>G XP_011522643.1:p.Pro417=
XM_005257058.4:c.1449C>G XP_005257115.2:p.Pro483=
XM_005257059.4:c.957+1581C>G XP_005257116.2:n.957+1581C>G
NM_000088.4:c.1449C>G MANE Select NP_000079.2:p.Pro483=
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