Canonical Allele Identifier: CA2670937307

Gene: ALB

Linked Data

• gnomAD v4: 4-73409290-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409290T>C , CM000666.2:g.73409290T>C	GRCh38
NC_000004.11:g.74275007T>C , CM000666.1:g.74275007T>C	GRCh37
NC_000004.10:g.74493871T>C	NCBI36
NG_009291.1:g.10036T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-65T>C MANE Select	ENSP00000295897.4:n.483-65T>C
ENST00000295897.8:c.483-65T>C	ENSP00000295897.4:n.483-65T>C
ENST00000401494.7:c.138-65T>C	ENSP00000384695.3:n.138-65T>C
ENST00000415165.6:c.138-2706T>C	ENSP00000401820.2:n.138-2706T>C
ENST00000441319.5:c.489-65T>C	ENSP00000392541.1:n.489-65T>C
ENST00000476441.6:c.80-65T>C	ENSP00000423727.1:n.80-65T>C
ENST00000503124.5:c.33-65T>C	ENSP00000421027.1:n.33-65T>C
ENST00000505649.5:n.169-65T>C
ENST00000509063.5:c.483-65T>C	ENSP00000422784.1:n.483-65T>C
ENST00000514786.1:n.452-65T>C
ENST00000621085.4:c.483-65T>C	ENSP00000483421.1:n.483-65T>C
ENST00000621628.4:c.486+214T>C	ENSP00000480485.1:n.486+214T>C
NM_000477.5:c.483-65T>C	NP_000468.1:n.483-65T>C
NM_000477.6:c.483-65T>C	NP_000468.1:n.483-65T>C
NM_000477.7:c.483-65T>C MANE Select	NP_000468.1:n.483-65T>C