Canonical Allele Identifier: CA508257747

Gene: BICRA

Linked Data

• MyVariant Identifiers: chr19:g.48183774C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47680517C>G , CM000681.2:g.47680517C>G	GRCh38
NC_000019.9:g.48183774C>G , CM000681.1:g.48183774C>G	GRCh37
NC_000019.8:g.52875586C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000594866.3:c.1347C>G MANE Select	ENSP00000469738.2:p.Val449=
ENST00000614245.2:c.621C>G	ENSP00000480219.2:p.Val207=
ENST00000396720.7:c.1347C>G	ENSP00000379946.2:p.Val449=
ENST00000614245.1:c.1191C>G	ENSP00000480219.1:p.Val397=
NM_015711.3:c.1347C>G	NP_056526.3:p.Val449=
XM_005258833.3:c.1347C>G	XP_005258890.1:p.Val449=
XM_006723180.2:c.1347C>G	XP_006723243.1:p.Val449=
XM_011526882.1:c.1209C>G	XP_011525184.1:p.Val403=
XM_011526883.1:c.1347C>G	XP_011525185.1:p.Val449=
XM_005258833.4:c.1347C>G	XP_005258890.1:p.Val449=
XM_006723180.3:c.1347C>G	XP_006723243.1:p.Val449=
XM_011526882.2:c.1209C>G	XP_011525184.1:p.Val403=
XM_011526883.2:c.1347C>G	XP_011525185.1:p.Val449=
NM_001394372.1:c.1347C>G MANE Select	NP_001381301.1:p.Val449=