Canonical Allele Identifier: CA400213514
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 526866
ClinVar RCV Id: RCV000631496
dbSNP Id: rs1555573288
MyVariant Identifiers: chr17:g.48269890C>T (hg19) chr17:g.50192529C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192529C>T , CM000679.2:g.50192529C>T GRCh38
NC_000017.10:g.48269890C>T , CM000679.1:g.48269890C>T GRCh37
NC_000017.9:g.45624889C>T NCBI36
NG_007400.1:g.14111G>A , LRG_1:g.14111G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1930-1G>A MANE Select ENSP00000225964.6:n.1930-1G>A
ENST00000225964.9:c.1930-1G>A ENSP00000225964.5:n.1930-1G>A
ENST00000476387.1:n.279-1G>A
NM_000088.3:c.1930-1G>A , LRG_1t1:c.1930-1G>A NP_000079.2:n.1930-1G>A
XM_005257058.3:c.1930-1G>A XP_005257115.2:n.1930-1G>A
XM_005257059.3:c.1012-1G>A XP_005257116.2:n.1012-1G>A
XM_011524341.1:c.1732-1G>A XP_011522643.1:n.1732-1G>A
XM_005257058.4:c.1930-1G>A XP_005257115.2:n.1930-1G>A
XM_005257059.4:c.1012-1G>A XP_005257116.2:n.1012-1G>A
NM_000088.4:c.1930-1G>A MANE Select NP_000079.2:n.1930-1G>A
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