Canonical Allele Identifier: CA2980220
Gene: BMP2K HGNC NCBI

Linked Data

dbSNP Id: rs143594573
gnomAD v2: 4-79786867-A-T
gnomAD v3: 4-78865713-A-T
gnomAD v4: 4-78865713-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78865713A>T , CM000666.2:g.78865713A>T GRCh38
NC_000004.11:g.79786867A>T , CM000666.1:g.79786867A>T GRCh37
NC_000004.10:g.80005891A>T NCBI36
NG_047162.1:g.94336A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000502613.3:c.1224A>T MANE Select ENSP00000424668.2:p.Arg408Ser
ENST00000335016.9:c.1224A>T ENSP00000334836.5:p.Arg408Ser
ENST00000389010.7:c.*200A>T ENSP00000373662.3:n.*200A>T
ENST00000502613.1:c.301A>T
ENST00000502871.5:c.1224A>T ENSP00000421768.1:p.Arg408Ser
ENST00000505725.1:n.506A>T
ENST00000628286.1:c.*200A>T ENSP00000487317.1:n.*200A>T
NM_017593.3:c.1224A>T NP_060063.2:p.Arg408Ser
NM_198892.1:c.1224A>T NP_942595.1:p.Arg408Ser
XM_005263117.1:c.1224A>T XP_005263174.1:p.Arg408Ser
XM_011532101.1:c.984A>T XP_011530403.1:p.Arg328Ser
XM_011532102.1:c.1224A>T XP_011530404.1:p.Arg408Ser
XM_017008381.1:c.984A>T XP_016863870.1:p.Arg328Ser
XM_017008382.1:c.336A>T XP_016863871.1:p.Arg112Ser
NM_017593.4:c.1224A>T NP_060063.2:p.Arg408Ser
NM_017593.5:c.1224A>T NP_060063.2:p.Arg408Ser
NM_198892.2:c.1224A>T MANE Select NP_942595.1:p.Arg408Ser