Canonical Allele Identifier: CA800319909
Gene: BMPR1B HGNC NCBI

Linked Data

dbSNP Id: rs1335368742
gnomAD v3: 4-94935416-G-T
gnomAD v4: 4-94935416-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935416G>T , CM000666.2:g.94935416G>T GRCh38
NC_000004.11:g.95856567G>T , CM000666.1:g.95856567G>T GRCh37
NC_000004.10:g.96075590G>T NCBI36
NG_009245.1:g.182440G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515059.6:c.-113+59516G>T MANE Select ENSP00000426617.1:n.-113+59516G>T
ENST00000515059.5:c.-113+59516G>T ENSP00000426617.1:n.-113+59516G>T
NM_001203.2:c.-113+59516G>T NP_001194.1:n.-113+59516G>T
XM_011532201.1:c.-18+59516G>T XP_011530503.1:n.-18+59516G>T
XM_011532201.2:c.-18+59516G>T XP_011530503.1:n.-18+59516G>T
XM_017008558.1:c.-113+59516G>T XP_016864047.1:n.-113+59516G>T
XM_017008559.1:c.-113+36366G>T XP_016864048.1:n.-113+36366G>T
NM_001203.3:c.-113+59516G>T MANE Select NP_001194.1:n.-113+59516G>T