Canonical Allele Identifier: CA406612901

Gene: BICRA

Linked Data

• gnomAD v4: 19-47680525-T-C
• MyVariant Identifiers: chr19:g.48183782T>C (hg19) ; chr19:g.47680525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47680525T>C , CM000681.2:g.47680525T>C	GRCh38
NC_000019.9:g.48183782T>C , CM000681.1:g.48183782T>C	GRCh37
NC_000019.8:g.52875594T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000594866.3:c.1355T>C MANE Select	ENSP00000469738.2:p.Leu452Pro
ENST00000614245.2:c.629T>C	ENSP00000480219.2:p.Leu210Pro
ENST00000396720.7:c.1355T>C	ENSP00000379946.2:p.Leu452Pro
ENST00000614245.1:c.1199T>C	ENSP00000480219.1:p.Leu400Pro
NM_015711.3:c.1355T>C	NP_056526.3:p.Leu452Pro
XM_005258833.3:c.1355T>C	XP_005258890.1:p.Leu452Pro
XM_006723180.2:c.1355T>C	XP_006723243.1:p.Leu452Pro
XM_011526882.1:c.1217T>C	XP_011525184.1:p.Leu406Pro
XM_011526883.1:c.1355T>C	XP_011525185.1:p.Leu452Pro
XM_005258833.4:c.1355T>C	XP_005258890.1:p.Leu452Pro
XM_006723180.3:c.1355T>C	XP_006723243.1:p.Leu452Pro
XM_011526882.2:c.1217T>C	XP_011525184.1:p.Leu406Pro
XM_011526883.2:c.1355T>C	XP_011525185.1:p.Leu452Pro
NM_001394372.1:c.1355T>C MANE Select	NP_001381301.1:p.Leu452Pro