Canonical Allele Identifier: CA406616964

Gene: BICRA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47681276G>C , CM000681.2:g.47681276G>C	GRCh38
NC_000019.9:g.48184533G>C , CM000681.1:g.48184533G>C	GRCh37
NC_000019.8:g.52876345G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594866.3:c.2106G>C MANE Select	ENSP00000469738.2:p.Gln702His
ENST00000614245.2:c.1380G>C	ENSP00000480219.2:p.Gln460His
ENST00000396720.7:c.2106G>C	ENSP00000379946.2:p.Gln702His
ENST00000614245.1:c.1950G>C	ENSP00000480219.1:p.Gln650His
NM_015711.3:c.2106G>C	NP_056526.3:p.Gln702His
XM_005258833.3:c.2106G>C	XP_005258890.1:p.Gln702His
XM_006723180.2:c.2106G>C	XP_006723243.1:p.Gln702His
XM_011526882.1:c.1968G>C	XP_011525184.1:p.Gln656His
XM_011526883.1:c.2106G>C	XP_011525185.1:p.Gln702His
XM_005258833.4:c.2106G>C	XP_005258890.1:p.Gln702His
XM_006723180.3:c.2106G>C	XP_006723243.1:p.Gln702His
XM_011526882.2:c.1968G>C	XP_011525184.1:p.Gln656His
XM_011526883.2:c.2106G>C	XP_011525185.1:p.Gln702His
NM_001394372.1:c.2106G>C MANE Select	NP_001381301.1:p.Gln702His