Canonical Allele Identifier: CA406313917
Gene: BCAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45315482G>A (hg19) chr19:g.44812225G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44812225G>A , CM000681.2:g.44812225G>A GRCh38
NC_000019.9:g.45315482G>A , CM000681.1:g.45315482G>A GRCh37
NC_000019.8:g.50007322G>A NCBI36
NG_007480.1:g.8145G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270233.12:c.267G>A MANE Select ENSP00000270233.5:p.Gln89=
ENST00000591520.6:c.205-1G>A ENSP00000467100.2:n.205-1G>A
ENST00000611077.5:c.267G>A ENSP00000481153.1:p.Gln89=
ENST00000270233.10:c.267G>A ENSP00000270233.5:p.Gln89=
ENST00000588603.1:n.262G>A
ENST00000589651.5:c.267G>A ENSP00000476710.1:p.Gln89=
ENST00000591520.5:c.205-1G>A ENSP00000467100.1:n.205-1G>A
ENST00000611077.4:c.267G>A ENSP00000481153.1:p.Gln89=
NM_001013257.2:c.267G>A NP_001013275.1:p.Gln89=
NM_005581.4:c.267G>A NP_005572.2:p.Gln89=
NM_005581.5:c.267G>A MANE Select NP_005572.2:p.Gln89=
Search 100 bp 5'
Search 100 bp 3'