Canonical Allele Identifier: CA2671157182

Gene: BMP2K

Linked Data

• dbSNP Id: rs1292084836
• gnomAD v4: 4-78865812-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865812T>C , CM000666.2:g.78865812T>C	GRCh38
NC_000004.11:g.79786966T>C , CM000666.1:g.79786966T>C	GRCh37
NC_000004.10:g.80005990T>C	NCBI36
NG_047162.1:g.94435T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1231+92T>C MANE Select	ENSP00000424668.2:n.1231+92T>C
ENST00000335016.9:c.1231+92T>C	ENSP00000334836.5:n.1231+92T>C
ENST00000389010.7:c.*207+92T>C	ENSP00000373662.3:n.*207+92T>C
ENST00000502613.1:c.308+92T>C
ENST00000502871.5:c.1231+92T>C	ENSP00000421768.1:n.1231+92T>C
ENST00000628286.1:c.*207+92T>C	ENSP00000487317.1:n.*207+92T>C
NM_017593.3:c.1231+92T>C	NP_060063.2:n.1231+92T>C
NM_198892.1:c.1231+92T>C	NP_942595.1:n.1231+92T>C
XM_005263117.1:c.1231+92T>C	XP_005263174.1:n.1231+92T>C
XM_011532101.1:c.991+92T>C	XP_011530403.1:n.991+92T>C
XM_011532102.1:c.1231+92T>C	XP_011530404.1:n.1231+92T>C
XM_017008381.1:c.991+92T>C	XP_016863870.1:n.991+92T>C
XM_017008382.1:c.343+92T>C	XP_016863871.1:n.343+92T>C
NM_017593.4:c.1231+92T>C	NP_060063.2:n.1231+92T>C
NM_017593.5:c.1231+92T>C	NP_060063.2:n.1231+92T>C
NM_198892.2:c.1231+92T>C MANE Select	NP_942595.1:n.1231+92T>C