Canonical Allele Identifier: CA102292615
Gene: BMPR1B HGNC NCBI

Linked Data

dbSNP Id: rs911684894
MyVariant Identifiers: chr4:g.95856645G>A (hg19) chr4:g.94935494G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935494G>A , CM000666.2:g.94935494G>A GRCh38
NC_000004.11:g.95856645G>A , CM000666.1:g.95856645G>A GRCh37
NC_000004.10:g.96075668G>A NCBI36
NG_009245.1:g.182518G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59594G>A MANE Select ENSP00000426617.1:n.-113+59594G>A
ENST00000515059.5:c.-113+59594G>A ENSP00000426617.1:n.-113+59594G>A
NM_001203.2:c.-113+59594G>A NP_001194.1:n.-113+59594G>A
XM_011532201.1:c.-18+59594G>A XP_011530503.1:n.-18+59594G>A
XM_011532201.2:c.-18+59594G>A XP_011530503.1:n.-18+59594G>A
XM_017008558.1:c.-113+59594G>A XP_016864047.1:n.-113+59594G>A
XM_017008559.1:c.-113+36444G>A XP_016864048.1:n.-113+36444G>A
NM_001203.3:c.-113+59594G>A MANE Select NP_001194.1:n.-113+59594G>A
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