Canonical Allele Identifier: CA14921767

Gene: BCR

Linked Data

• dbSNP Id: rs373334393
• gnomAD v2: 22-23627475-A-T
• gnomAD v3: 22-23285288-A-T
• gnomAD v4: 22-23285288-A-T
• MyVariant Identifiers: chr22:g.23627475A>T (hg19) ; chr22:g.23285288A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285288A>T , CM000684.2:g.23285288A>T	GRCh38
NC_000022.10:g.23627475A>T , CM000684.1:g.23627475A>T	GRCh37
NC_000022.9:g.21957475A>T	NCBI36
NG_009244.1:g.109924A>T
NG_009244.2:g.109924A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+87A>T MANE Select	ENSP00000303507.8:n.2406+87A>T
ENST00000305877.12:c.2406+87A>T	ENSP00000303507.8:n.2406+87A>T
ENST00000359540.7:c.2406+87A>T	ENSP00000352535.3:n.2406+87A>T
ENST00000398512.9:c.1270-2856A>T	ENSP00000381524.6:n.1270-2856A>T
ENST00000466076.1:n.480+87A>T
ENST00000487968.5:n.1059+87A>T
NM_004327.3:c.2406+87A>T	NP_004318.3:n.2406+87A>T
NM_021574.2:c.2406+87A>T	NP_067585.2:n.2406+87A>T
XR_001755448.1:n.1050T>A
NM_004327.4:c.2406+87A>T MANE Select	NP_004318.3:n.2406+87A>T
NM_021574.3:c.2406+87A>T	NP_067585.2:n.2406+87A>T