Canonical Allele Identifier: CA415920337
Gene: MASP2 HGNC NCBI

Linked Data

gnomAD v4: 1-11046900-G-A
MyVariant Identifiers: chr1:g.11106957G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11046900G>A , CM000663.2:g.11046900G>A GRCh38
NC_000001.10:g.11106957G>A , CM000663.1:g.11106957G>A GRCh37
NC_000001.9:g.11029544G>A NCBI36
NG_007289.1:g.5329C>T
NG_007289.2:g.5329C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699958.1:c.225C>T ENSP00000514717.1:p.Asp75=
ENST00000700088.1:c.225C>T ENSP00000514787.1:p.Asp75=
ENST00000700089.1:c.225C>T ENSP00000514788.1:p.Asp75=
ENST00000700090.1:c.225C>T ENSP00000514789.1:p.Asp75=
ENST00000700091.1:c.225C>T ENSP00000514790.1:p.Asp75=
ENST00000700092.1:c.225C>T ENSP00000514791.1:p.Asp75=
ENST00000700093.1:c.225C>T ENSP00000514792.1:p.Asp75=
ENST00000700094.1:c.225C>T ENSP00000514793.1:p.Asp75=
ENST00000700095.1:c.225C>T ENSP00000514794.1:p.Asp75=
ENST00000700096.1:c.225C>T ENSP00000514795.1:p.Asp75=
ENST00000700097.1:c.225C>T ENSP00000514796.1:p.Asp75=
ENST00000400897.8:c.225C>T MANE Select ENSP00000383690.3:p.Asp75=
ENST00000400897.7:c.225C>T ENSP00000383690.3:p.Asp75=
ENST00000400898.3:c.225C>T ENSP00000383691.3:p.Asp75=
ENST00000480221.1:n.245C>T
NM_006610.3:c.225C>T NP_006601.2:p.Asp75=
NM_139208.2:c.225C>T NP_631947.1:p.Asp75=
XM_017000097.1:c.225C>T XP_016855586.1:p.Asp75=
XR_001736931.1:n.257C>T
XR_001736932.1:n.257C>T
XR_002958895.1:n.257C>T
NM_006610.4:c.225C>T MANE Select NP_006601.2:p.Asp75=
NM_139208.3:c.225C>T NP_631947.1:p.Asp75=