Canonical Allele Identifier: CA508257683
Gene: BICRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48183684G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47680427G>A , CM000681.2:g.47680427G>A GRCh38
NC_000019.9:g.48183684G>A , CM000681.1:g.48183684G>A GRCh37
NC_000019.8:g.52875496G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000594866.3:c.1257G>A MANE Select ENSP00000469738.2:p.Leu419=
ENST00000614245.2:c.531G>A ENSP00000480219.2:p.Leu177=
ENST00000396720.7:c.1257G>A ENSP00000379946.2:p.Leu419=
ENST00000614245.1:c.1101G>A ENSP00000480219.1:p.Leu367=
NM_015711.3:c.1257G>A NP_056526.3:p.Leu419=
XM_005258833.3:c.1257G>A XP_005258890.1:p.Leu419=
XM_006723180.2:c.1257G>A XP_006723243.1:p.Leu419=
XM_011526882.1:c.1119G>A XP_011525184.1:p.Leu373=
XM_011526883.1:c.1257G>A XP_011525185.1:p.Leu419=
XM_005258833.4:c.1257G>A XP_005258890.1:p.Leu419=
XM_006723180.3:c.1257G>A XP_006723243.1:p.Leu419=
XM_011526882.2:c.1119G>A XP_011525184.1:p.Leu373=
XM_011526883.2:c.1257G>A XP_011525185.1:p.Leu419=
NM_001394372.1:c.1257G>A MANE Select NP_001381301.1:p.Leu419=