Canonical Allele Identifier: CA508257752
Gene: BICRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48183781C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47680524C>T , CM000681.2:g.47680524C>T GRCh38
NC_000019.9:g.48183781C>T , CM000681.1:g.48183781C>T GRCh37
NC_000019.8:g.52875593C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000594866.3:c.1354C>T MANE Select ENSP00000469738.2:p.Leu452=
ENST00000614245.2:c.628C>T ENSP00000480219.2:p.Leu210=
ENST00000396720.7:c.1354C>T ENSP00000379946.2:p.Leu452=
ENST00000614245.1:c.1198C>T ENSP00000480219.1:p.Leu400=
NM_015711.3:c.1354C>T NP_056526.3:p.Leu452=
XM_005258833.3:c.1354C>T XP_005258890.1:p.Leu452=
XM_006723180.2:c.1354C>T XP_006723243.1:p.Leu452=
XM_011526882.1:c.1216C>T XP_011525184.1:p.Leu406=
XM_011526883.1:c.1354C>T XP_011525185.1:p.Leu452=
XM_005258833.4:c.1354C>T XP_005258890.1:p.Leu452=
XM_006723180.3:c.1354C>T XP_006723243.1:p.Leu452=
XM_011526882.2:c.1216C>T XP_011525184.1:p.Leu406=
XM_011526883.2:c.1354C>T XP_011525185.1:p.Leu452=
NM_001394372.1:c.1354C>T MANE Select NP_001381301.1:p.Leu452=