Canonical Allele Identifier: CA1477857884
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935536_94935540delinsAAATC , CM000666.2:g.94935536_94935540delinsAAATC GRCh38
NC_000004.11:g.95856687_95856691delinsAAATC , CM000666.1:g.95856687_95856691delinsAAATC GRCh37
NC_000004.10:g.96075710_96075714delinsAAATC NCBI36
NG_009245.1:g.182560_182564delinsAAATC

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59636_-113+59640delinsAAATC MANE Select ENSP00000426617.1:n.-113+59636_-113+59640...
ENST00000515059.5:c.-113+59636_-113+59640delinsAAATC ENSP00000426617.1:n.-113+59636_-113+59640...
NM_001203.2:c.-113+59636_-113+59640delinsAAATC NP_001194.1:n.-113+59636_-113+59640delins...
XM_011532201.1:c.-18+59636_-18+59640delinsAAATC XP_011530503.1:n.-18+59636_-18+59640delin...
XM_011532201.2:c.-18+59636_-18+59640delinsAAATC XP_011530503.1:n.-18+59636_-18+59640delin...
XM_017008558.1:c.-113+59636_-113+59640delinsAAATC XP_016864047.1:n.-113+59636_-113+59640del...
XM_017008559.1:c.-113+36486_-113+36490delinsAAATC XP_016864048.1:n.-113+36486_-113+36490del...
NM_001203.3:c.-113+59636_-113+59640delinsAAATC MANE Select NP_001194.1:n.-113+59636_-113+59640delins...