Canonical Allele Identifier: CA500844305
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48265484G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188123G>C , CM000679.2:g.50188123G>C GRCh38
NC_000017.10:g.48265484G>C , CM000679.1:g.48265484G>C GRCh37
NC_000017.9:g.45620483G>C NCBI36
NG_007400.1:g.18517C>G , LRG_1:g.18517C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3234C>G MANE Select ENSP00000225964.6:p.Val1078=
ENST00000225964.9:c.3234C>G ENSP00000225964.5:p.Val1078=
ENST00000486572.1:n.432C>G
ENST00000511732.1:n.558C>G
NM_000088.3:c.3234C>G , LRG_1t1:c.3234C>G NP_000079.2:p.Val1078=
XM_005257058.3:c.2964C>G XP_005257115.2:p.Val988=
XM_005257059.3:c.2316C>G XP_005257116.2:p.Val772=
XM_011524341.1:c.3036C>G XP_011522643.1:p.Val1012=
XM_005257058.4:c.2964C>G XP_005257115.2:p.Val988=
XM_005257059.4:c.2316C>G XP_005257116.2:p.Val772=
NM_000088.4:c.3234C>G MANE Select NP_000079.2:p.Val1078=