Canonical Allele Identifier: CA357238075

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275097C>G (hg19) ; chr4:g.73409380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409380C>G , CM000666.2:g.73409380C>G	GRCh38
NC_000004.11:g.74275097C>G , CM000666.1:g.74275097C>G	GRCh37
NC_000004.10:g.74493961C>G	NCBI36
NG_009291.1:g.10126C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.508C>G MANE Select	ENSP00000295897.4:p.His170Asp
ENST00000295897.8:c.508C>G	ENSP00000295897.4:p.His170Asp
ENST00000401494.7:c.163C>G	ENSP00000384695.3:p.His55Asp
ENST00000415165.6:c.138-2616C>G	ENSP00000401820.2:n.138-2616C>G
ENST00000441319.5:c.514C>G	ENSP00000392541.1:p.His172Asp
ENST00000476441.6:c.105C>G	ENSP00000423727.1:p.Asp35Glu
ENST00000503124.5:c.58C>G	ENSP00000421027.1:p.His20Asp
ENST00000505649.5:n.194C>G
ENST00000509063.5:c.508C>G	ENSP00000422784.1:p.His170Asp
ENST00000511370.1:c.41C>G
ENST00000514786.1:n.477C>G
ENST00000621085.4:c.490+18C>G	ENSP00000483421.1:n.490+18C>G
ENST00000621628.4:c.486+304C>G	ENSP00000480485.1:n.486+304C>G
NM_000477.5:c.508C>G	NP_000468.1:p.His170Asp
NM_000477.6:c.508C>G	NP_000468.1:p.His170Asp
NM_000477.7:c.508C>G MANE Select	NP_000468.1:p.His170Asp