Canonical Allele Identifier: CA587232
Gene: MASP2 HGNC NCBI

Linked Data

dbSNP Id: rs763695031
gnomAD v2: 1-11106974-G-A
gnomAD v3: 1-11046917-G-A
gnomAD v4: 1-11046917-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11046917G>A , CM000663.2:g.11046917G>A GRCh38
NC_000001.10:g.11106974G>A , CM000663.1:g.11106974G>A GRCh37
NC_000001.9:g.11029561G>A NCBI36
NG_007289.1:g.5312C>T
NG_007289.2:g.5312C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699958.1:c.208C>T ENSP00000514717.1:p.His70Tyr
ENST00000700088.1:c.208C>T ENSP00000514787.1:p.His70Tyr
ENST00000700089.1:c.208C>T ENSP00000514788.1:p.His70Tyr
ENST00000700090.1:c.208C>T ENSP00000514789.1:p.His70Tyr
ENST00000700091.1:c.208C>T ENSP00000514790.1:p.His70Tyr
ENST00000700092.1:c.208C>T ENSP00000514791.1:p.His70Tyr
ENST00000700093.1:c.208C>T ENSP00000514792.1:p.His70Tyr
ENST00000700094.1:c.208C>T ENSP00000514793.1:p.His70Tyr
ENST00000700095.1:c.208C>T ENSP00000514794.1:p.His70Tyr
ENST00000700096.1:c.208C>T ENSP00000514795.1:p.His70Tyr
ENST00000700097.1:c.208C>T ENSP00000514796.1:p.His70Tyr
ENST00000400897.8:c.208C>T MANE Select ENSP00000383690.3:p.His70Tyr
ENST00000400897.7:c.208C>T ENSP00000383690.3:p.His70Tyr
ENST00000400898.3:c.208C>T ENSP00000383691.3:p.His70Tyr
ENST00000480221.1:n.228C>T
NM_006610.3:c.208C>T NP_006601.2:p.His70Tyr
NM_139208.2:c.208C>T NP_631947.1:p.His70Tyr
XM_017000097.1:c.208C>T XP_016855586.1:p.His70Tyr
XR_001736931.1:n.240C>T
XR_001736932.1:n.240C>T
XR_002958895.1:n.240C>T
NM_006610.4:c.208C>T MANE Select NP_006601.2:p.His70Tyr
NM_139208.3:c.208C>T NP_631947.1:p.His70Tyr