Canonical Allele Identifier: CA342629887
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571199A>C , CM000663.2:g.154571199A>C GRCh38
NC_000001.10:g.154543675A>C , CM000663.1:g.154543675A>C GRCh37
NC_000001.9:g.152810299A>C NCBI36
NG_008027.1:g.8419A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.376A>C MANE Select ENSP00000357461.3:p.Met126Leu
ENST00000636034.1:c.376A>C ENSP00000489703.1:p.Met126Leu
ENST00000637900.1:c.382A>C ENSP00000490474.1:p.Met128Leu
ENST00000368476.3:c.376A>C ENSP00000357461.3:p.Met126Leu
NM_000748.2:c.376A>C NP_000739.1:p.Met126Leu
XM_017000180.2:c.-9-126A>C XP_016855669.1:n.-9-126A>C
XR_001736952.2:n.628A>C
NM_000748.3:c.376A>C MANE Select NP_000739.1:p.Met126Leu